for Pharma & Biotech
We have access to a global network of more than 100 industry experts with wide-ranging specialisms so if you do not see your chosen topic in this catalogue, simply get in touch and we will be happy to develop the training for you.
Module 3 of the Global CTD
eCTD Submissions
EU Regulatory Affairs
US-FDA Drug Submission Procedures
Filing Variations
Pharmaceutical Regulatory Affairs in China
Regulatory Affairs in the Mena Region
Gaining Marketing Authorisations in CIS
Regulatory Affairs in Latin America
EU & US Requirements for Pharmacuetical Labelling & Packaging
Regulatory Affairs for Clinical Trials
Project Management for Regulatory Affairs Professionals
Regulatory Affairs Strategies
Regulatory Risk Management
Drug/Device Combination Products
Regulatory and Development Strategies for Generics
Regulatory Affairs for Veterinary Medicine
Regulatory, Developmental and Manufacturing Challenges for Cell & Gene Therapies
Regulatory Information Management and IDMP Training
GDPR and Data Protection for the Pharmaceutical Industry