Our Services
TECHNOLOGY TRANSFER
We specialise in offering companies manufacturing know-how and product dossiers to meet international Regulatory. Authorities’ registration requirements, with the objective of facilitating the supply of basic generic medicines at a reasonable cost.
AUDITING
Meditech is able to undertake independent assessment of clients’ facilities and operations against published GMP guidelines, and carry out third party audits where contract manufacture or importation is being considered.
CONSULTANCY
We can provide comprehensive and pragmatic advice to assist clients to comply with official guidelines and regulations. This can cover:
new and upgraded facility designs
selection and procurement of plant and equipment
introduction of new products and processes
manufacturing authorisation applications
preparation for regulatory inspections
quality management systems
TRAINING
We can provide in-house training to maintain high standards of QA and GMP, and for the introduction of new products and process technologies.
VALIDATION
We can provide logical and cost-effective approaches to equipment and process validation, which will meet all QA and GMP requirements.
CONTACTS
To complement the in-house expertise within Meditech, we have access to a broad range of specialised skills, such as:
facilities design and build
cost and project management
engineering and validation services
product registration
formulation development and trouble shooting
Bioprogress stock quotes
Bioprogress stock charts
Follow this thread
