PGF offers thorough Quality Control (QC) management for your finished pharmaceutical products, ensuring compliance and quality through a structured process and extensive resources.

• Access to a Wide European Network: We provide access to a large network of test laboratories located throughout Europe.
• Client-Focused Laboratory Selection: The selection of the specific laboratory is made in agreement with you, the client. Key factors considered include price, proven reliability, speed of service, and the available capacities relevant to your product’s testing needs.
• Dedicated QC Testing: Our partner pharmaceutical testing laboratories are equipped to carry out the necessary quality control tests directly on your finished pharmaceutical products.
• Adherence to Your Procedures: All tests are performed strictly according to the registered analytical procedures that are provided by you, the client.
• Formal Certification: We ensure that Certificates Of Analysis (COA) are issued based on the agreed-upon release specifications for your product.
• Managed Analytical Method Transfer: When required, analytical method transfer is carried out. This process follows a collaborative selection approach designed to best suit the needs and capabilities of both the receiving laboratory and the transferring laboratory.

To facilitate the QC process, our service encompasses:

• Documentation Support: Offering to provide necessary documentation, such as protocols and reports.
• Resource Procurement: Management of equipment and consumables procurement needed for the analytical work.
• Advanced Process Capability: Utilization of state-of-the-art GLC (Gas-Liquid Chromatography) processes where applicable for analysis.