Upholding rigorous quality standards is not only a regulatory imperative but also vital for ensuring the efficacy and safety of pharmaceutical products. And as many pharma manufacturers have discovered, enhanced quality processes can also unlock significant performance improvements.
But quality improvements do not come without challenges, as drugmakers must contend with complex global supply chains, evolving regulatory requirements and the unique quality considerations of novel therapies.
In this eBook you will gain insight on:
- How to use CAPA to support continuous process improvement
- How real-time metrics can drive proactive quality management
- Key considerations for CGMP raw materials compliance
- Cutting-edge technologies that enhance equipment validation
Sponsored by: IFC, IQVIA Technologies, Blue Mountain Quality Resources, Novartis Pharma AG