Understanding and Preparing the Quality and Pharmaceutical Module 2014 is a course that provides tools on how to:
Ensure that Module 3 (CTD - Common Technical Document) of your dossier contains all data needed
Compile and submit Module 3 (CTD) of your registration dossier
Deal effectively with regulators
Achieve the quickest turnaround of your submission
Who should Attend
Compliance Managers
Regulatory Affairs Managers/Officers/ Assistants
Product Registration Personnel
Documentation Managers
Qualified Persons
Project Managers in Regulatory Affairs
Key contributors to the submission package
Past Events
Understanding and Preparing the Quality and Pharmaceutical Module 2014 - 22-24 Jan 2014, Radisson Blu Edwardian Grafton Hotel, London, United Kingdom (40935)
Understanding and Preparing the Quality and Pharmaceutical Module of the Global CTD Dossier July 2011 - 12-14 Jul 2011, MWB Victoria, London, United Kingdom (15759)
Understanding and Preparing the Quality and Pharmaceutical Module 2026
Important
Please, check "Understanding and Preparing the Quality and Pharmaceutical Module" official website for possible changes, before making any traveling arrangements
