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: 

 

tl_files/events/andrew.jpgAndrew Marr, PhD,
Managing Director at Marr Consultancy Ltd
Speaker Bio

 

 

tl_files/events/Sinisa Belina.jpgSiniša 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

Sponsored by INFOTEHNA

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