PHARMACEUTICAL 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 troubleshooting