UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
PURSUANT
TO SECTION 13 OR 15(d)
OF THE SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported): November 5, 2014
OraSure Technologies, Inc.
(Exact Name of Registrant as Specified in Charter)
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| Delaware |
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001-16537 |
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36-4370966 |
| (State or Other Jurisdiction
of Incorporation) |
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(Commission
File Number) |
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(I.R.S. Employer
Identification No.) |
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| 220 East First Street |
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18015-1360 |
| Bethlehem, Pennsylvania
(Address of Principal Executive Offices) |
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(Zip Code) |
Registrant’s telephone number, including area code: 610-882-1820
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the Registrant under any of the
following provisions:
| ¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
| ¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
| ¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
| ¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Item 2.02 – Results of Operations and Financial Condition.
On November 5, 2014, OraSure Technologies, Inc. (the “Company”) issued a press release announcing its consolidated financial results for the
quarter ended September 30, 2014, and providing financial guidance for the fourth quarter of 2014. A copy of the press release is attached as Exhibit 99.1 to this Form 8-K and is incorporated herein by reference.
The information in this Item and attached Exhibit shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934
or otherwise subject to the liabilities of that section, nor shall such information and Exhibit be deemed incorporated by reference in any filing under the Securities Act of 1933, except as shall be expressly set forth by specific reference in such
a filing. The fact that the information and Exhibit are being furnished should not be deemed an admission as to the materiality of any information contained therein. The Company undertakes no duty or obligation to publicly update or revise the
information contained in this Current Report or attached Exhibit.
Item 7.01 – Regulation FD Disclosure.
On November 5, 2014, the Company held a webcast conference call with analysts and investors, during which Douglas A. Michels, the Company’s President
and Chief Executive Officer, and Ronald H. Spair, the Company’s Chief Financial Officer and Chief Operating Officer, discussed the Company’s consolidated financial results for the quarter ended September 30, 2014, provided financial
guidance for the fourth quarter of 2014 and described certain business developments. A copy of the prepared remarks of Messrs. Michels and Spair is attached as Exhibit 99.2 to this Form 8-K and is incorporated herein by reference.
The information in this Item and attached Exhibit shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934
or otherwise subject to the liabilities of that section, nor shall such information and Exhibit be deemed incorporated by reference in any filing under the Securities Act of 1933, except as shall be expressly set forth by specific reference in such
a filing. The fact that the information and Exhibit are being furnished should not be deemed an admission as to the materiality of any information contained therein. The Company undertakes no duty or obligation to publicly update or revise the
information contained in this Current Report or attached Exhibit.
Item 9.01 – Financial Statements and Exhibits.
(d) Exhibits
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Exhibit Number |
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Description |
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99.1 |
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Press Release, dated November 5, 2014, announcing consolidated financial results of OraSure Technologies, Inc. for the quarter ended September 30, 2014, and providing financial guidance for the fourth quarter of
2014. |
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99.2 |
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Prepared Remarks of Douglas A. Michels and Ronald H. Spair for OraSure Technologies, Inc. Third Quarter 2014 Analyst/ Investor Conference Call Held November 5, 2014. |
Signatures
Pursuant to the requirements of the Securities and Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf
by the undersigned, hereunto duly authorized.
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ORASURE TECHNOLOGIES, INC. |
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| Date: November 5, 2014 |
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By: |
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/s/ Jack E. Jerrett |
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Jack E. Jerrett |
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Senior Vice President, General Counsel |
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and Secretary |
Index to Exhibits
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| Exhibit No. |
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Description |
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| 99.1 |
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Press Release, dated November 5, 2014, announcing consolidated financial results of OraSure Technologies, Inc. for the quarter ended September 30, 2014, and providing financial guidance for the fourth quarter of
2014. |
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| 99.2 |
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Prepared Remarks of Douglas A. Michels and Ronald H. Spair for OraSure Technologies, Inc. Third Quarter 2014 Analyst/ Investor Conference Call Held November 5, 2014. |
Exhibit 99.1
Company Contact:
Ronald H.
Spair
Chief Financial Officer
610-882-1820
Investorinfo@orasure.com
www.orasure.com
OraSure Announces 2014 Third Quarter Financial Results
BETHLEHEM, PA – November 5, 2014 – (Globe Newswire) – OraSure Technologies, Inc. (NASDAQ: OSUR), a market leader in oral fluid
diagnostics, today announced its consolidated financial results for the three and nine months ended September 30, 2014.
Financial Highlights
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• |
|
Consolidated net revenues for the third quarter of 2014 were $27.8 million, a 13% increase from the comparable quarter of 2013. Consolidated net revenues for the nine months ended September 30, 2014 were $77.8
million, an 11% increase from the comparable period of 2013. |
| |
• |
|
Net revenues for the Company’s OraQuick® rapid HCV test in the domestic marketplace were $1.3 million and $3.2 million for the third quarter and first
nine months of 2014, respectively, representing a 99% and 80% increase over the third quarter and first nine months of 2013, respectively. |
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• |
|
Net revenues generated by DNAG were $6.9 million and $17.5 million for the third quarter and first nine months of 2014, respectively, representing a 38% and 29% increase over the third quarter and first nine months of
2013, respectively. |
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• |
|
Licensing and product development revenues were $3.4 million and $4.2 million for the quarter and nine months ended September 30, 2014, respectively, and represent the recognition of payments under the
Company’s’ HCV collaboration with AbbVie. |
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• |
|
Consolidated net income for the third quarter of 2014 was $1.1 million, or $0.02 per share on a fully diluted basis, which compares to a net loss of $1.9 million, or $0.03 per share, for the third quarter of 2013.
Consolidated net loss for the nine months ended September 30, 2014 was $2.0 million, or $0.04 per share, which compares to a net loss of $17.4 million, or $0.31 per share, for the comparable period of 2013. |
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• |
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Cash resources totaled $98.9 million at September 30, 2014 and working capital amounted to $104.8 million. |
“We are very pleased with the Company’s financial performance for the third quarter,” said Douglas A. Michels, President and CEO of OraSure
Technologies. “Our molecular collection systems business achieved a record level of revenues, our OraQuick® HCV business has continued to grow and we reported a consolidated net profit
for the second quarter in a row. We also continued to make great progress in the execution of our HCV collaboration with AbbVie, which will help drive continued growth in future periods.”
Financial Results
Consolidated net product revenues for
the third quarter of 2014 remained flat at $24.5 million. Consolidated net product revenues for the nine month period ended September 30, 2014 increased 6% over the prior year period, primarily as a result of higher sales of the Company’s
molecular collection systems, OraQuick® HCV and cryosurgical systems products. These increases were partially offset by lower sales of the
OraQuick® professional HIV product and OraQuick® HIV In-Home test, and lower substance abuse and insurance risk assessment product
sales.
Consolidated licensing and product development revenues for the third quarter and first nine months of 2014 were $3.4 million and $4.2 million,
respectively. Consolidated licensing and product development revenues for the third quarter and first nine months of 2013 were $147,000 and $623,000, respectively. Licensing and product development revenues in 2014 represent the recognition of
payments under the Company’s HCV collaboration agreement with AbbVie. Licensing and product development revenues in 2013 represent royalties paid on domestic outsales of Merck’s OTC cryosurgical wart removal product, pursuant to a license
and settlement agreement that expired in 2013.
Consolidated gross margin for the three and nine months ended September 30, 2014 was 67% and 63%,
respectively. Consolidated gross margin for the three and nine months ended September 30, 2013 was 61% and 59%, respectively. Gross margin for the current quarter and nine-month period improved largely as a result of the higher licensing and
product development revenues and a more favorable product mix resulting from higher margin DNAG sales.
2
Consolidated operating expenses increased to $17.8 million during the third quarter of 2014 compared to $17.0
million in the comparable period of 2013. For the nine months ended September 30, 2014, consolidated operating expenses were $50.9 million, a decrease from the $59.7 million reported for the nine months ended September 30, 2013. The
increase in the third quarter of 2014 was primarily related to higher research and development supply costs and higher staffing, legal and consulting expenses. The decrease for the nine-month period of 2014 was primarily due to a favorable $5.5
million contract termination payment from Roche Diagnostics, lower promotional expenses associated with the Company’s OraQuick® In-Home HIV test and decreased research and development
expenses due to lower clinical trial and staffing costs. Promotional expenses for the OraQuick® In-Home test were $7.7 million and $14.2 million for the first nine months of 2014 and 2013,
respectively. General and administrative expenses in the nine-month period increased due to higher legal, staffing and consulting costs.
For the three
and nine months ended September, 2014, the Company recorded Canadian income tax expense of $10,000 and a Canadian income tax benefit of $33,000, respectively. For the three and nine months ended September 30, 2013, the Company recorded Canadian
income tax benefits of $127,000 and $786,000, respectively. The tax benefits were recorded as a result of certain Canadian research and development and investment tax credits and, for the 2013 periods, DNAG’s loss before income taxes.
The Company’s cash and short-term investment balance totaled $98.9 million at September 30, 2014 compared to $93.2 million in cash at
December 31, 2013. Working capital was $104.8 million at September 30, 2014 compared to $100.6 million at December 31, 2013. For the nine months ended September 30, 2014, the Company’s operations generated $8.4 million of
cash.
Fourth Quarter 2014 Outlook
The Company
expects consolidated net revenues to range from $28.0 to $28.5 million and is projecting a consolidated net loss of approximately $0.04 to $0.05 per share for the fourth quarter of 2014.
3
Financial Data
Condensed Consolidated Financial Data
(In thousands, except per-share data)
Unaudited
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Three months ended
September 30, |
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Nine months ended
September 30, |
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2014 |
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2013 |
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2014 |
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2013 |
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| Results of Operations |
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| Net revenues |
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$ |
27,845 |
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$ |
24,671 |
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$ |
77,783 |
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$ |
70,172 |
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| Cost of products sold |
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9,140 |
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9,738 |
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29,135 |
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28,711 |
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| Gross profit |
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18,705 |
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14,933 |
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48,648 |
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41,461 |
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| Operating expenses: |
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| Research and development |
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2,990 |
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|
2,670 |
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8,242 |
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|
8,720 |
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| Sales and marketing |
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9,216 |
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8,981 |
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30,828 |
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35,224 |
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| General and administrative |
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5,617 |
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5,342 |
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17,317 |
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15,742 |
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| Gain on contract termination settlement |
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— |
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— |
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(5,500 |
) |
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— |
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| Total operating expenses |
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17,823 |
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|
16,993 |
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|
50,887 |
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59,686 |
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| Operating income (loss) |
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|
882 |
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|
(2,060 |
) |
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|
(2,239 |
) |
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|
(18,225 |
) |
| Other income |
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|
268 |
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|
41 |
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|
244 |
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36 |
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|
|
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|
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|
|
|
|
|
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|
|
|
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| Income (loss) before income taxes |
|
|
1,150 |
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|
(2,019 |
) |
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|
(1,995 |
) |
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|
(18,189 |
) |
| Income tax expense (benefit) |
|
|
10 |
|
|
|
(127 |
) |
|
|
(33 |
) |
|
|
(786 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net income (loss) |
|
$ |
1,140 |
|
|
$ |
(1,892 |
) |
|
$ |
(1,962 |
) |
|
$ |
(17,403 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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| Earnings (loss) per share: |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Basic |
|
$ |
0.02 |
|
|
$ |
(0.03 |
) |
|
$ |
(0.04 |
) |
|
$ |
(0.31 |
) |
|
|
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|
|
|
|
|
|
|
|
|
|
|
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| Diluted |
|
$ |
0.02 |
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|
$ |
(0.03 |
) |
|
$ |
(0.04 |
) |
|
$ |
(0.31 |
) |
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| Weighted average shares: |
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| Basic |
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|
56,018 |
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|
|
55,592 |
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|
|
55,897 |
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|
55,534 |
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|
|
|
|
|
|
|
|
|
|
|
|
|
|
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|
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| Diluted |
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|
56,666 |
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|
55,592 |
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|
|
55,897 |
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|
|
55,534 |
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4
Summary of Revenues by Market and Product (Unaudited)
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Three Months Ended September 30, |
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Dollars |
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Percentage of
Total Net
Revenues |
|
| Market |
|
2014 |
|
|
2013 |
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%
Change |
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2014 |
|
|
2013 |
|
| Infectious disease testing |
|
$ |
11,183 |
|
|
$ |
12,873 |
|
|
|
(13 |
)% |
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|
40 |
% |
|
|
52 |
% |
| Substance abuse testing |
|
|
2,149 |
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|
2,092 |
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|
3 |
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|
8 |
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|
8 |
|
| Cryosurgical systems |
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|
3,241 |
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|
3,649 |
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(11 |
) |
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11 |
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15 |
|
| Molecular collection systems |
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|
6,867 |
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|
4,964 |
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|
38 |
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|
25 |
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|
20 |
|
| Insurance risk assessment |
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|
1,007 |
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|
946 |
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|
6 |
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|
4 |
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|
4 |
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|
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|
|
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| Net product revenues |
|
|
24,447 |
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|
|
24,524 |
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|
|
— |
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|
88 |
|
|
|
99 |
|
| Licensing and product development |
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|
3,398 |
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|
147 |
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NM |
* |
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12 |
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|
1 |
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|
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|
|
|
|
|
|
|
|
|
|
|
|
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| Net revenues |
|
$ |
27,845 |
|
|
$ |
24,671 |
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|
|
13 |
% |
|
|
100 |
% |
|
|
100 |
% |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
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|
|
|
|
|
| |
|
Nine Months Ended September 30, |
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| |
|
Dollars |
|
|
|
|
|
Percentage of
Total Net
Revenues |
|
| Market |
|
2014 |
|
|
2013 |
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|
%
Change |
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|
2014 |
|
|
2013 |
|
| Infectious disease testing |
|
$ |
34,914 |
|
|
$ |
35,526 |
|
|
|
(2 |
)% |
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|
45 |
% |
|
|
51 |
% |
| Substance abuse testing |
|
|
6,187 |
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|
|
6,455 |
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|
(4 |
) |
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|
8 |
|
|
|
9 |
|
| Cryosurgical systems |
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|
12,128 |
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|
|
10,910 |
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|
|
11 |
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|
|
15 |
|
|
|
16 |
|
| Molecular collection systems |
|
|
17,523 |
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|
|
13,550 |
|
|
|
29 |
|
|
|
23 |
|
|
|
19 |
|
| Insurance risk assessment |
|
|
2,858 |
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|
|
3,108 |
|
|
|
(8 |
) |
|
|
4 |
|
|
|
4 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net product revenues |
|
|
73,610 |
|
|
|
69,549 |
|
|
|
6 |
|
|
|
95 |
|
|
|
99 |
|
| Licensing and product development |
|
|
4,173 |
|
|
|
623 |
|
|
|
NM |
* |
|
|
5 |
|
|
|
1 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net revenues |
|
$ |
77,783 |
|
|
$ |
70,172 |
|
|
|
11 |
% |
|
|
100 |
% |
|
|
100 |
% |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
* Calculation is not considered meaningful.
5
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|
|
|
|
|
|
|
|
|
| |
|
Three Months Ended
September 30, |
|
|
Nine Months Ended
September 30, |
|
| OraQuick® Revenues |
|
2014 |
|
|
2013 |
|
|
%
Change |
|
|
2014 |
|
|
2013 |
|
|
%
Change |
|
| Domestic HIV |
|
$ |
7,231 |
|
|
$ |
8,093 |
|
|
|
(11 |
)% |
|
$ |
21,568 |
|
|
$ |
23,854 |
|
|
|
(10 |
)% |
| International HIV |
|
|
491 |
|
|
|
1,157 |
|
|
|
(58 |
) |
|
|
1,897 |
|
|
|
2,457 |
|
|
|
(23 |
) |
| Domestic HIV OTC |
|
|
1,368 |
|
|
|
1,762 |
|
|
|
(22 |
) |
|
|
4,991 |
|
|
|
5,196 |
|
|
|
(4 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net HIV revenues |
|
|
9,090 |
|
|
|
11,012 |
|
|
|
(17 |
) |
|
|
28,456 |
|
|
|
31,507 |
|
|
|
(10 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Domestic HCV |
|
|
1,301 |
|
|
|
653 |
|
|
|
99 |
|
|
|
3,183 |
|
|
|
1,772 |
|
|
|
80 |
|
| International HCV |
|
|
470 |
|
|
|
924 |
|
|
|
(49 |
) |
|
|
2,341 |
|
|
|
1,409 |
|
|
|
66 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net HCV revenues |
|
|
1,771 |
|
|
|
1,577 |
|
|
|
12 |
|
|
|
5,524 |
|
|
|
3,181 |
|
|
|
74 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net OraQuick®revenues |
|
$ |
10,861 |
|
|
$ |
12,589 |
|
|
|
(14 |
)% |
|
$ |
33,980 |
|
|
$ |
34,688 |
|
|
|
(2 |
)% |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
Three Months Ended
September 30, |
|
|
Nine Months Ended
September 30, |
|
| Intercept® Revenues |
|
2014 |
|
|
2013 |
|
|
%
Change |
|
|
2014 |
|
|
2013 |
|
|
%
Change |
|
| Domestic |
|
$ |
1,606 |
|
|
$ |
1,495 |
|
|
|
7 |
% |
|
$ |
4,473 |
|
|
$ |
4,240 |
|
|
|
5 |
% |
| International |
|
|
3 |
|
|
|
29 |
|
|
|
(90 |
) |
|
|
76 |
|
|
|
385 |
|
|
|
(80 |
) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net Intercept®revenues |
|
$ |
1,609 |
|
|
$ |
1,524 |
|
|
|
6 |
% |
|
$ |
4,549 |
|
|
$ |
4,625 |
|
|
|
(2 |
)% |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
Three Months Ended
September 30, |
|
|
Nine Months Ended
September 30, |
|
| Cryosurgical Systems Revenues |
|
2014 |
|
|
2013 |
|
|
%
Change |
|
|
2014 |
|
|
2013 |
|
|
%
Change |
|
| Domestic professional |
|
$ |
1,590 |
|
|
$ |
1,803 |
|
|
|
(12 |
)% |
|
$ |
4,601 |
|
|
$ |
4,192 |
|
|
|
10 |
% |
| International professional |
|
|
43 |
|
|
|
435 |
|
|
|
(90 |
) |
|
|
581 |
|
|
|
1,039 |
|
|
|
(44 |
) |
| International over-the-counter |
|
|
1,608 |
|
|
|
1,411 |
|
|
|
14 |
|
|
|
6,946 |
|
|
|
5,679 |
|
|
|
22 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| Net cryosurgical systems revenues |
|
$ |
3,241 |
|
|
$ |
3,649 |
|
|
|
(11 |
)% |
|
$ |
12,128 |
|
|
$ |
10,910 |
|
|
|
11 |
% |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
6
Condensed Consolidated Balance Sheets (Unaudited)
|
|
|
|
|
|
|
|
|
| |
|
September 30, 2014 |
|
|
December 31, 2013 |
|
| Assets |
|
|
|
|
|
|
|
|
| Cash |
|
$ |
93,855 |
|
|
$ |
93,191 |
|
| Short-term investments |
|
|
5,000 |
|
|
|
— |
|
| Accounts receivable, net |
|
|
14,920 |
|
|
|
12,957 |
|
| Inventories |
|
|
14,843 |
|
|
|
11,444 |
|
| Other current assets |
|
|
1,429 |
|
|
|
1,983 |
|
| Property and equipment, net |
|
|
17,958 |
|
|
|
17,933 |
|
| Intangible assets, net |
|
|
18,831 |
|
|
|
22,226 |
|
| Goodwill |
|
|
22,562 |
|
|
|
23,782 |
|
| Other non-current assets |
|
|
1,102 |
|
|
|
729 |
|
|
|
|
|
|
|
|
|
|
| Total assets |
|
$ |
190,500 |
|
|
$ |
184,245 |
|
|
|
|
|
|
|
|
|
|
| Liabilities and Stockholders’ Equity |
|
|
|
|
|
|
|
|
| Accounts payable |
|
$ |
4,510 |
|
|
$ |
4,834 |
|
| Deferred revenue |
|
|
11,540 |
|
|
|
1,119 |
|
| Accrued expenses |
|
|
9,203 |
|
|
|
13,032 |
|
| Other non-current liabilities |
|
|
1,090 |
|
|
|
677 |
|
| Deferred income taxes |
|
|
3,233 |
|
|
|
3,437 |
|
| Stockholders’ equity |
|
|
160,924 |
|
|
|
161,146 |
|
|
|
|
|
|
|
|
|
|
| Total liabilities and stockholders’ equity |
|
$ |
190,500 |
|
|
$ |
184,245 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| |
|
Nine months ended
September 30, |
|
| Additional Financial Data (Unaudited) |
|
2014 |
|
|
2013 |
|
| Capital expenditures |
|
$ |
2,353 |
|
|
$ |
1,696 |
|
| Depreciation and amortization |
|
$ |
4,732 |
|
|
$ |
4,846 |
|
| Stock based compensation |
|
$ |
4,284 |
|
|
$ |
4,187 |
|
| Cash provided by (used in) operating activities |
|
$ |
8,384 |
|
|
$ |
(3,142 |
) |
Conference Call
The
Company will host a conference call and audio webcast to discuss the Company’s 2014 third quarter financial results, certain business developments and financial guidance for the fourth quarter of 2014, beginning today at 5:00 p.m. Eastern Time
(2:00 p.m. Pacific Time). On the call will be Douglas A. Michels, President and Chief Executive Officer and Ronald H. Spair, Chief Financial Officer and Chief Operating Officer. The call will include prepared remarks by management and a question and
answer session.
7
In order to listen to the conference call, please either dial 844-831-3030 (Domestic) or 315-625-6887
(International) and reference Conference ID #17659442 or go to OraSure Technologies’ web site, www.orasure.com, and click on the Investor Relations page. Please click on the webcast link and follow the prompts for registration and access
10 minutes prior to the call. A replay of the call will be archived on OraSure Technologies’ web site shortly after the call has ended and will be available for seven days. A replay of the call can also be accessed until November 12, 2014,
by dialing 855-859-2056 (Domestic) or 404-537-3406 (International) and entering the Conference ID #17659442.
About OraSure Technologies
OraSure Technologies is a leader in the development, manufacture and distribution of oral fluid diagnostic and collection devices and other technologies
designed to detect or diagnose critical medical conditions. Its innovative products include rapid tests for the detection of antibodies to HIV and HCV at the point of care and testing solutions for detecting various drugs of abuse. The Company sells
the OraQuick® In-Home HIV Test, the first and only rapid HIV test approved by the U.S. Food and Drug Administration for sale to the consumer over-the-counter market in the U.S. In addition,
the Company is a leading provider of oral fluid sample collection, stabilization and preparation products for molecular diagnostic applications. OraSure’s portfolio of products is sold globally to various clinical laboratories, hospitals,
clinics, community-based organizations and other public health organizations, research and academic institutions, distributors, government agencies, physicians’ offices, and commercial and industrial entities. The Company’s products enable
healthcare providers to deliver critical information to patients, empowering them to make decisions to improve and protect their health. For more information on the Company, please visit www.orasure.com
Important Information
This press release contains
certain forward-looking statements, including with respect to expected revenues and earnings/loss per share. Forward-looking statements are not guarantees of future performance or results. Known and unknown factors that could cause actual
performance or results to be materially different from those expressed or implied in these statements include, but are not limited to: ability to market and sell products, whether through our internal, direct sales force or third parties; ability to
manufacture products in accordance with applicable specifications, performance standards and quality requirements; ability to obtain, and timing and cost of obtaining, necessary regulatory approvals for new products or new indications or
applications for existing products; ability to comply with applicable regulatory requirements; ability to effectively resolve warning letters, audit observations and other findings or comments from the FDA or other regulators; changes in
relationships, including disputes or disagreements, with strategic partners or other parties and reliance on strategic partners for the performance of critical activities under collaborative arrangements; our ability to achieve financial and
performance objectives under the HCV collaboration with AbbVie; failure of distributors or other customers to meet purchase forecasts, historic purchase levels or minimum purchase requirements for our products; impact of replacing distributors;
inventory levels at distributors and other customers;
8
ability of DNA Genotek to achieve its financial and strategic objectives and continue to increase its revenues; ability to identify, complete, integrate and realize the full benefits of future
acquisitions; impact of competitors, competing products and technology changes; impact of negative economic conditions, high unemployment and poor credit conditions; reduction or deferral of public funding available to customers; competition from
new or better technology or lower cost products; ability to develop, commercialize and market new products, including the OraQuick® In-Home HIV test; market acceptance of oral fluid testing or
other products; changes in market acceptance of products based on product performance or other factors, including changes in CDC or other testing guidelines, algorithms or other recommendations; ability to fund research and development and other
products and operations; ability to obtain and maintain new or existing product distribution channels; reliance on sole supply sources for critical products and components; availability of related products produced by third parties or products
required for use of our products; history of losses and ability to achieve sustained profitability; ability to utilize net operating loss carry forwards or other deferred tax assets; volatility of OraSure’s stock price; uncertainty relating to
patent protection and potential patent infringement claims; uncertainty and costs of litigation relating to patents and other intellectual property; availability of licenses to patents or other technology; ability to enter into international
manufacturing agreements; obstacles to international marketing and manufacturing of products; ability to sell products internationally, including the impact of changes in international funding sources and testing algorithms; adverse movements in
foreign currency exchange rates; loss or impairment of sources of capital; ability to attract and retain qualified personnel; exposure to product liability and other types of litigation; changes in international, federal or state laws and
regulations; customer consolidations and inventory practices; equipment failures and ability to obtain needed raw materials and components; the impact of terrorist attacks and civil unrest; and general political, business and economic conditions.
These and other factors are discussed more fully in the Company’s Securities and Exchange Commission filings, including its registration statements, Annual Report on Form 10-K for the year ended December 31, 2013, Quarterly Reports on Form
10-Q, and other filings with the SEC. Although forward-looking statements help to provide information about future prospects, readers should keep in mind that forward-looking statements may not be reliable. The forward-looking statements are made as
of the date of this press release and OraSure Technologies undertakes no duty to update these statements.
# # #
9
Exhibit 99.2
OraSure Technologies, Inc.
2014 Third Quarter
Analyst/Investor Conference Call
November 5, 2014
Prepared Remarks of Douglas A. Michels and Ronald H. Spair
Please see “Important Information” at the conclusion of the following prepared remarks.
Introduction – Doug Michels
Thanks
Rena. Good afternoon everyone and welcome to our call.
I am pleased to report that we had a very successful and extremely productive third quarter. Our
financial performance exceeded our guidance on both the top and bottom lines and we believe this continues the momentum that has been building for most of this year.
| |
• |
|
Consolidated net revenues for the quarter were $27.8 million, a 13% increase from Q3 of 2013. |
| |
• |
|
Our molecular collection systems business turned in another record quarter with almost $7 million in revenues, a 38% increase over the prior year period. |
| |
• |
|
Our HCV business also delivered solid results with sales growth of about 12% over Q3 2013. Domestic sales revenue doubled over Q3 2013. In addition, we recorded $3.4 million in licensing and product development revenue
related to this business line as a result of our HCV collaboration with AbbVie. |
| |
• |
|
We are also pleased to report a consolidated net profit for the quarter of $1.1 million. |
As you might expect,
a main focus during the past few months has been the launch of our collaboration with AbbVie and the co-promotion of our OraQuick® HCV Rapid Antibody Test. Our initiatives in several
markets are now well under way and good progress has been made to increase awareness and train potential customers on our product with the goal of stimulating additional testing. Much has been
accomplished and there is still much work to be completed as we finish the year and move into 2015.
Later in the call, I will provide more detail on our
HCV collaboration activities as well as on developments at DNA Genotek. I will also touch briefly on our efforts to develop a rapid point-of-care test for Ebola on our OraQuick® platform.
So with that brief introduction, let me turn the call over to Ron for his financial review.
Third Quarter 2014 Financial Results – Ron Spair
Thanks Doug, and good afternoon everyone.
Revenues
– Ron Spair
Our third quarter 2014 consolidated net revenues were $27.8 million, an increase of 13% over the $24.7 million reported in
2013. Our consolidated product revenues of $24.5 million were unchanged when compared to the comparable period of 2013. Higher sales from our molecular collection systems business and domestic OraQuick® HCV product were offset by lower sales of
our OraQuick® professional HIV and cryosurgical systems products and a reduction in OraQuick® In-Home HIV test sales. Licensing and product development revenues were $3.4 million in the
current quarter compared to $147,000 in 2013.
Sales of our OraQuick® HCV professional product in
the domestic market increased 99% in Q3 to $1.3 million from $653,000 in the prior year. Higher demand among new and existing customers was the primary reason for this increase. International sales of our HCV test in the third quarter of 2014
decreased to $470,000 from $924,000 in the same period last year, primarily due to reduced
- 2 -
sales in support of a testing program with an international NGO which made its first stocking purchase in the third quarter of 2013. We expect sales to this NGO to continue at a reduced rate in
Q4.
Our overall infectious disease testing revenues decreased 13% to $11.2 million in the third quarter of 2014, compared to $12.9 million in the
third quarter of 2013. Domestic sales of our professional HIV product decreased to $7.2 million in the third quarter of 2014 from $8.1 million in the third quarter of 2013. This decrease was the result of customer migration to automated 4th generation HIV immunoassays as recommended under new testing guidelines issued by the CDC, and continued pressure on government budgets. We expect continued pressure on our professional HIV business
for the foreseeable future.
International sales of our professional HIV product decreased to $491,000 in the third quarter of 2014 from $1.2 million in
the third quarter of 2013, primarily due to the timing of product shipments in support of a significant African testing program.
During the current
quarter, net sales of our OraQuick® In-Home HIV test were $1.4 million compared to $1.8 million in the third quarter of 2013. Net revenues for these periods were not recorded using the same
revenue recognition policy and are not readily comparable. So a better way to evaluate the performance of this product is to look at the number of units purchased by consumers. Available point-of-sale data shows unit consumption remained flat in the
third quarter of 2014 compared to the third quarter of 2013.
As you may recall, we previously announced that we would implement a new promotional
strategy for the In-home HIV test that is focused on more cost-effective methods of building awareness and consumer adoption at retail. Under this strategy, we have largely stopped the expensive broad-based consumer
- 3 -
advertising, and instead have adopted a lower cost and more economical promotional approach geared towards the retail or trade environment. This new approach has substantially reduced our
promotional spend for this product.
Third quarter 2014 cryosurgical revenues decreased 11% to $3.2 million from $3.6 million in the third quarter of
2013, primarily as a result of lower sales of our professional product in both the U.S. and international markets partially offset by higher OTC sales in Europe. Domestic professional sales decreased to $1.6 million in the third quarter of 2014 from
$1.8 million in the third quarter of 2013 due to the impact of the merger of our two largest distributors who began selling a competing private label cryosurgical product. Professional sales in the international markets decreased to $43,000 from
$435,000 in the third quarter of 2014 and 2013, respectively, as we experienced delivery problems and inventory shortages as we transitioned to a new manufacturer of Histofreezer®.
OTC cyrosurgical sales increased to $1.6 million in the third quarter of 2014 from $1.4 million in the third quarter of 2013, largely due to customer ordering
patterns.
Our molecular collection systems revenues, primarily representing sales of the
Oragene® product line, increased to $6.9 million in the third quarter of 2014 compared to $5.0 million in 2013. This 38% increase was the result of higher sales in the both the academic and
commercial markets.
Licensing and product development revenues were $3.4 million in the third quarter of 2014 and represent the recognition of revenues
from AbbVie under our HCV collaboration agreement. Third quarter 2013 licensing and product development revenues were $147,000 and represent royalties paid on domestic outsales of Merck’s OTC cryosurgical wart removal product.
- 4 -
Gross Margin – Ron Spair
Gross margin for the third quarter of 2014 was 67% compared to 61% reported for the third quarter of 2013. The current quarter margin benefited primarily from
the $3.4 million of licensing and product development revenues recognized from our AbbVie relationship as well as a more favorable product mix driven largely by increased DNAG sales to higher margin customers.
Operating Expenses – Ron Spair
Our
consolidated operating expenses for the third quarter of 2014 increased to $17.8 million compared to $17.0 million in the third quarter of 2013. This increase was primarily related to higher R&D costs associated with qualifying a new raw
material vendor and higher staffing, legal and consulting expenses.
Net Income – Ron Spair
From a bottom line perspective, we reported net income of $1.1 million, or $0.02 per share on a fully-diluted basis, for the third quarter of 2014, compared to
a net loss of $1.9 million, or $0.03 per share, for the same period of 2013.
Cash Flow from Operations and Liquidity – Ron
Spair
Turning briefly to our balance sheet and cash flow, we continue to maintain a solid cash and liquidity position. Our cash and short-term
investment balance at September 30, 2014 was $98.9 million compared to $93.2 million at December 31, 2013. Cash generated by operating activities in the third quarter of 2014 was $18.8 million compared to $6.1 million generated in the
third quarter of 2013. The primary reason for this improvement was the $15.0 million payment received from AbbVie in the third quarter.
- 5 -
Fourth Quarter 2014 Consolidated Financial Guidance – Ron Spair
Turning to guidance for the fourth quarter of 2014, we are projecting consolidated net revenues of approximately $28.0 to $28.5 million and a consolidated
net loss per share of approximately $0.04 to $0.05 for the quarter. The projected net loss reflects higher operating expenses driven by two main factors. First, we expect increased R&D spending during Q4 on our drug assay development program
with Thermo for our next generation Intercept oral fluid collector and on our Ebola feasibility efforts. Second, Q4 sales and marketing expenses will also be up as a result of increased spending in support of the AbbVie collaboration.
As we look further out, we expect to continue somewhat higher spending as a result of the AbbVie collaboration, the next generation Intercept device and the
Ebola development work I just mentioned.
From a product revenue perspective, we anticipate that the intra-year revenue distribution for 2015 will be much
like 2014 with Q1 being down sequentially and then building strongly from there.
And, with that, I will now turn the call back over to Doug.
Business Update – Doug Michels
Thanks, Ron.
OraQuick® HCV – Doug Michels
I would like to begin our business discussion with HCV.
Implementing our HCV collaboration with AbbVie continues to be a top priority. You may recall that our co-promotion efforts are focused on several key
markets in the U.S. We are pleased with the progress to date.
- 6 -
One of our largest initiatives is focused on primary care and specialty physicians, and was launched
approximately 10 weeks ago. Over that time period, the AbbVie sales force has been detailing our OraQuick® HCV test to physicians and we have launched a comprehensive training program for this
customer segment. Our detailing efforts to date have resulted in well over 1,000 physicians indicating a strong interest in the product. We are seeing a high rate of purchase intent once a physician or physician office completes our training
program. Our representatives are tasked with making sure product pull through occurs following the completion of customer training. It has been our experience that once a physician’s office expresses interest in our product, it takes three to
four weeks to schedule training. Following the training, it then takes another three to four weeks for the first product order and the commencement of testing. Consequently, we are just beginning to see the impact from these efforts on our sales
line. Our expectation is that sales will continue to grow, but meaningful results will not materialize until 2015. We are extremely encouraged by the results we are seeing in this initiative so far.
We are also encouraged by the fact that product interest is being generated across a variety of practices, ranging from multi-site physician offices, internal
medicine practices, practices that service HIV patients, corrections facilities and community health centers. In addition, we are finding that the prevalence rate for HCV runs higher in some practices than the average for the baby boomer population
of 3%. In a pilot conducted in one large U.S. jail system, we saw a prevalence of 7%. Similarly, offices that serve HIV patients have substantially higher prevalence rates. We are also seeing testing volumes at some of these customers range from
10,000 – 20,000 tests annually, which approaches the volumes of some of our larger public health accounts.
We certainly believe we are off to a
solid start with this initiative. Our representatives will continue to coordinate with their AbbVie counterparts on all aspects of this physician co-promotion initiative.
- 7 -
The second primary initiative targets employers or employer groups with employees that are at high risk for
hepatitis C. The initial focus here has been on commercial long-haul truck drivers. .
We have been working closely with the Healthy Trucking Association
of America, or HTAA, along with an organization known as Rolling Strong. Both of these groups collaborate and focus on improving the health and wellness of professional truck drivers. OraSure and AbbVie are specifically promoting the use of our test
in physician offices, health clinics and retail pharmacies where truckers receive their health care, at driving schools where newly-hired drivers are required to take and pass a physical exam, and at health events sponsored by HTAA and Rolling
Strong where truckers can take advantage of a variety of health and wellness services. We are also engaging in discussions with large fleet owners. We have assembled a Fleet Advisory Board and will hold our first meeting next week. We have also
assembled a Clinical Advisory Board for this effort and that group will meet in December.
Our co-promotion efforts geared towards truckers began in
earnest with a major awareness and testing event at the Great American Truck Show in Dallas, Texas in late August. More recently, we have conducted other testing events at some of the larger truck stops in the United States, including stops located
in Carlisle, Pennsylvania and in Bordentown, New Jersey. Yesterday, we had an event at a large truck stop in Tampa, Florida and another event is planned later this year in Ontario, California. Similar events are expected throughout 2015. The primary
objective of these trucker shows is to educate and build awareness about HCV and to offer on-site rapid HCV testing along with the AbbVie patient support program. In conjunction with these events, OraSure and AbbVie are also in discussions with
several physician groups and organizations who provide health care services to a significant number of truck drivers.
- 8 -
A third major market segment consists of national and regional retail pharmacies and retail clinics. With the
increased focus on expanding health and diagnostic services to consumers, we believe local retail pharmacy outlets are an important growth area for our HCV collaboration. OraSure and AbbVie are continuing discussions with several major retail
pharmacies and health providers about increasing hepatitis awareness and making our OraQuick® HCV test and AbbVie’s Patient Care Model available through retail outlets. Good discussions
continue with a number of retailers and we hope to share more definitive progress updates in the months to come.
As previously discussed, the effort
required to adequately address these market segments is substantial. A great deal of work is required to build awareness, promote our test and implement the various support services that are needed, including product training, co-payment assistance
and patient support. We are implementing this collaboration as quickly as possible, and substantial progress has been made since we signed the AbbVie agreement in June. As I mentioned previously, we expect to see increased revenues from the
collaboration in Q4, but we are not projecting a significant financial impact from these efforts until 2015.
In addition to the AbbVie collaboration, we
continue to drive improvement in our existing HCV business. We achieved another record in Q3 with $1.3 million in domestic revenues. We shipped product to over 460 customers during the quarter, with 82% of our shipments being delivered to repeat
customers. We also added over 80 new customers during this period.
So, as we look forward, we anticipate continued progress in our HCV business. We
expect product sales to continue increasing, especially here in the U.S., and we expect to achieve some of the performance goals under our HCV collaboration with AbbVie next year.
- 9 -
Molecular Collection Systems – Doug Michels
Another area I want to address is our molecular collection systems business.
As noted earlier in the call, DNA Genotek delivered another record quarter in Q3, with $6.9 million in revenues, a 38% increase over the third quarter of last
year. DNA Genotek’s revenues for the quarter were fairly evenly split between sales to the academic and commercial markets. Academic revenue grew over 80% compared to the year ago period, while commercial revenue grew approximately 16%. We are
extremely pleased with the performance of our molecular collection systems business.
During our last call, we discussed two new product development
initiatives underway at DNA Genotek. The first product, Omnigene GutTM, will enable academic researchers to collect and stabilize fecal samples for gut microbiome analyses. The second product
line, consisting of Omnigene SputumTM and a preparation reagent called PrepIt MaxTM, are designed to improve collection, transport,
stabilization and processing of sputum samples used for tuberculosis testing. Much of our activities for these products are centered around ensuring that early versions are being provided to key opinion leaders in the relevant markets – which
is exactly what is happening. DNA Genotek employees have been connecting with many key opinion leaders around the world and the feedback to date on these products is very positive. We believe these products represent promising new opportunities and
we expect both will make important contributions to the future of our molecular collection systems business.
Rapid Ebola Test – Doug
Michels
A final area I want to discuss is our efforts to develop a rapid test for Ebola. As you may have heard, Dr. Margaret Hamburg,
Commissioner of the U.S. FDA visited our offices a couple of weeks ago to recognize the collaborative work we have done with the agency over the years in bringing innovative HIV and HCV tests to the market. This meeting had been set up some time ago
and was not related to the development of an Ebola test.
- 10 -
However, towards the end of our meeting several members of the media interviewed Dr. Hamburg and me, and a
question was asked if we had plans to develop an Ebola test. In response, I explained that we had been recently contacted by certain public and private entities about developing such a test and that we were evaluating whether our technology platform
could deliver the performance levels required for this product.
As I’m sure you understand, OraSure is interested in doing whatever it can to
benefit the public health, especially with something as urgent and critical as Ebola. We have formed a cross-functional team to manage this project, and are actively assessing the technical feasibility of an Ebola test on our OraQuick® platform.
Studies indicate that oral fluid is a good carrier of the Ebola antigen, so we are
optimistic about our ability to develop a product that will deliver the appropriate performance characteristics, while bringing the benefits of rapid, oral fluid based diagnostics to this situation. We have been actively engaged with several
government and other organizations, including the FDA, CDC, NIH, the World Health Organization and certain non-profit foundations, regarding all aspects of developing, validating, gaining emergency regulatory approval and deploying a rapid
diagnostic for Ebola. In cooperation with these organizations and others, we are also assessing the commercial opportunity represented by this test.
We
expect to achieve several key milestones on this project during the fourth quarter of this year and we will provide an update on our progress at the appropriate time.
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Conclusion
So, as you’ve just heard, there is no shortage of opportunities available to the Company, and we are keenly focused on the successful execution of the
initiatives I have outlined today.
We continue to be extremely enthusiastic about our molecular collection systems business and its growth opportunities.
Our HCV business posted a solid performance in Q3 and is poised for substantial growth in 2015 and beyond. We believe in our strategy to further advance each of these parts of our business. I am pleased with our overall progress and encouraged that
we are on the right path towards maximizing the value of the opportunities before us. I look forward to a successful fourth quarter and moving to full-year profitability in 2015.
And with that, I will now open the floor to your questions. Operator, please proceed.
* * * *
[Q&A session]
Final Conclusion – Doug Michels
Thank
you for participating on today’s call and for your continued interest in OraSure. Have a good afternoon and evening.
Important Information
This document contains certain forward-looking statements, including with respect to expected revenues and earnings/loss per share. Forward-looking
statements are not guarantees of future performance or results. Known and unknown factors that could cause actual performance or results to be materially different from those
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expressed or implied in these statements include, but are not limited to: ability to market and sell products, whether through our internal, direct sales force or third parties; ability to
manufacture products in accordance with applicable specifications, performance standards and quality requirements; ability to obtain, and timing and cost of obtaining, necessary regulatory approvals for new products or new indications or
applications for existing products; ability to comply with applicable regulatory requirements; ability to effectively resolve warning letters, audit observations and other findings or comments from the FDA or other regulators; changes in
relationships, including disputes or disagreements, with strategic partners or other parties and reliance on strategic partners for the performance of critical activities under collaborative arrangements; our ability to achieve financial and
performance objectives under the HCV collaboration with AbbVie; failure of distributors or other customers to meet purchase forecasts, historic purchase levels or minimum purchase requirements for our products; impact of replacing distributors;
inventory levels at distributors and other customers; ability of DNA Genotek to achieve its financial and strategic objectives and continue to increase its revenues; ability to identify, complete, integrate and realize the full benefits of future
acquisitions; impact of competitors, competing products and technology changes; impact of negative economic conditions, high unemployment and poor credit conditions; reduction or deferral of public funding available to customers; competition from
new or better technology or lower cost products; ability to develop, commercialize and market new products, including the OraQuick® In-Home HIV test; market acceptance of oral fluid testing or
other products; changes in market acceptance of products based on product performance or other factors, including changes in CDC or other testing guidelines, algorithms or other recommendations; ability to fund research and development and other
products and operations; ability to obtain and maintain new or existing product distribution channels; reliance on sole supply sources for critical products and components; availability of related products produced by third parties or products
required for use of our products; history of losses and ability to achieve sustained
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profitability; ability to utilize net operating loss carry forwards or other deferred tax assets; volatility of OraSure’s stock price; uncertainty relating to patent protection and potential
patent infringement claims; uncertainty and costs of litigation relating to patents and other intellectual property; availability of licenses to patents or other technology; ability to enter into international manufacturing agreements; obstacles to
international marketing and manufacturing of products; ability to sell products internationally, including the impact of changes in international funding sources and testing algorithms; adverse movements in foreign currency exchange rates; loss or
impairment of sources of capital; ability to attract and retain qualified personnel; exposure to product liability and other types of litigation; changes in international, federal or state laws and regulations; customer consolidations and inventory
practices; equipment failures and ability to obtain needed raw materials and components; the impact of terrorist attacks and civil unrest; and general political, business and economic conditions. These and other factors are discussed more fully in
the Company’s Securities and Exchange Commission filings, including its registration statements, Annual Report on Form 10-K for the year ended December 31, 2013, Quarterly Reports on Form 10-Q, and other filings with the SEC. Although
forward-looking statements help to provide information about future prospects, readers should keep in mind that forward-looking statements may not be reliable. The forward-looking statements are made as of the date of this Report, and we undertake
no duty to update these statements.
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