Explore all upcoming CMC related training courses and secure your seat or an in-house session.
Future events
CMC and Regulatory Requirements for Inhalation Drug Products
24. February 2026
Implement ISO 14971 requirements in medical device risk management.
Process Scale-up & Tech Transfer for Injectables
9. March 2026
This online training is a deep dive into QbD-implemented Process Scale-up, Technology Transfer and PV for sterile injectables.
CMC Statistics
16. March 2026
CMC Statistics training for pharma professionals — apply key statistical tools for validation, methods, and regulatory success. Accelerate approvals and avoid rejections.
CMC/Regulatory Affairs for Nucleic Acids
25. March 2026
This 3-day online course provides a deep dive into the critical aspects of CMC and Regulatory Affairs of nucleic acids.
CMC Regulatory Compliance for Biologics – A CMC approach to IMPD Walkthrough for Biologics
29. April 2026
This training is focused on CMC Regulatory Compliance for Biologics.
Other events
CMC for Antibody-Drug Conjugates: Strategies for Successful Development and Manufacturing
1. December 2025
Implement ISO 14971 requirements in medical device risk management.
Process Development of Solid Dosage Formulations
This 2-day training course will focus on the challenges of solid dosage forms development establishing an effective drug development program.
Bioequivalence and IVIVC
Unique online training focusing on bioequivalence, IVIVC, biowaiver guidelines and bioavailability.
CMC Module in Regulatory Submissions
Interactive training covering CMC Module in Regulatory Submissions. Gain the tools to ensure potency and regulatory success.
CMC Regulatory Requirements for Biosimilars
3-days of online training with Dr. Len Pattenden on CMC-compliant regulatory practices and quality assurance for Biosimilars.
CMC Regulatory Compliance for ATMPs
3-days of online training with Dr. Len Pattenden on CMC-compliant regulatory practices for ATMPs.