Learn how to improve manufacturing efficiency, maintain product quality and improve GMP compliance.
Most courses leverage ISPE Guidance documents produced by pharmaceutical manufacturing industry professionals. These guides provide the practical, "real world" information needed to build on best practices to meet and exceed current regulatory requirements.
- Pharmaceutical Water Generation (T04)
- Cleaning Validation Principles (T17)
- Facility Project Management in the Regulated Pharmaceutical Industry (T26)
- A GAMP® Approach to Data Integrity, Electronic Records and Signatures, and Operation of GxP Computerized Systems (T50) – New Course!
- Storage Delivery and Qualification of Pharmaceutical Waters (T23)
- Process Validation in Biotechnology Manufacturing (T32)
- Applying Quality Risk Management (QRM) (T42)