- Preparation of Site Master File

- Preparation and development of documentation for pharmaceutical manufacturing processes and auxiliary systems.

- Qualification of equipment. Implementation of protocols and reports of IQ, OQ and DR.

- Annual Product Report (APR), according to  European Guidelines.

- Validation of manufacturing processes, 
 maintenance, cleaning and analytical methods


- Quality Control
- Pharmaceutical Development
- Registry Files
- Readability tests
- Prices and reimbursments
- Others

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