The Process Validation for Biotechnological Products - EU edition covers topics such as:
- Process Qualification (DS & DP)
- Process Design (DS & DP)
- Ancillary Process Validation Studies
- Continued Process Verification (DS & DP)
The Process Validation for Biotechnological Products - EU edition brings together:
- CMC development program managers
- Process development scientists and managers
- Manufacturing managers
- Pharmaceutical development scientists and managers
- Heads of Quality Assurance
- QC and stability control managers
- Drug Regulatory Affairs managers