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)
Important
Please, check "Understanding and Preparing the Quality and Pharmaceutical Module" official website for possible changes, before making any traveling arrangements
