By admin That’s a crucial aspect of QC Pharma! Testing and validation of raw materials, intermediates, and finished products involve verifying their identity, purity, potency, and quality to ensure they meet specifications and regulatory requirements.
This includes:
1. Raw Materials: Testing for identity, purity, and quality before use in manufacturing.
2. Intermediates: Verifying the quality and purity of partially processed materials.
3. Finished Products: Conducting comprehensive testing, including:
– Identity and strength
– Purity and impurities
– Dissolution and release
– Stability and shelf-life
– Labeling and packaging verification
Validation of these tests ensures the methods are accurate, reliable, and consistent. This rigorous testing and validation process guarantees the final product is safe, effective, and meets regulatory standards. Would you like more details or have specific questions about this process?