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
Understanding and Preparing the Quality and Pharmaceutical Module 2014 is intended for:
- 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