Free Webinar: EVMPD Hot issues - insight in scope and format of information
February 28, 2012 -
Date: 28th February 2012
Time: 3PM London / 10AM New York
Duration: 60 Minutes
Price: FREE
Join us for an in-depth discussion on challenges in building, validating and submitting XEVPRM. Your hosts will be:
Andrew Marr, PhD,
Managing Director at Marr Consultancy Ltd
Speaker Bio
Siniša Belina, MSc. Pharm.,
Product development, Process improvement at INFOTEHNA Group LLC
Speaker Bio
Key Learning Objectives:
- Understanding EVMPD guidance documents
- EVMPD submission challenges and how to tackle them
- Identification of information and documents needed for successful EVMPD submission
- Using eMPDExpertTM to manage EVMPD information and build XEVPRM
Audience:
- CEO Level Executives
- Directors
- Regulatory Affairs managers
- Regulatory Affairs experts
- Regulatory Operations managers
- Regulatory Operation experts
- Pharmacovigilance managers
- Pharmacovigilance experts
- IT managers












