FREE XEVPRM WORKSHOP: Are you ready for July 2, 2012?

December 08, 2011 - Hotel Aristos, Zagreb, Croatia


Ensuring easy and timely submission of eXtended EudraVigilance Product Report Message (XEVPRM)


The European Medicines Agency issued the Regulation (EC) No 726/2004Electronic Submission of Information on Medicinal Products for Human Use by Marketing Authorisation Holders to the European Medicines Agency which requires that by July 2, 2012, information on medicinal products for human use authorized or registered in the Union is submitted electronically.

  • Learn all about the new Regulation - its content, essence and requirements
  • Get ready in time with INFOTEHNA XEVPRMExpertTM
  • Seize an opportunity to be ahead of your competition
  • Submit your EV Product Report Message easily and on time


AGENDA

09:00-09:30 Registration
09:30-10:00 New EU Pharmacovigilance legislation
Tatjana Ajhler-Đuretek, Head of Medical Affairs and Pharmacovigilance, Belupo
10:00-11:00 Electronic submission of information on medicinal products for human use: Overview and requirements
(Mihajlo Ceraj Ceric, Life Sciences Director and Sinisa Belina, Business Services Deputy Director)
11:00-11:30 Coffee break
11:30-12:30 Preparing XEVPRM the easy way with INFOTEHNA XEVPRMExpertTM 
(Elvis Pacelat, CEO)
12:30-13:00 How to simply implement XEVPRM tool INFOTEHNA XEVPRMExpertTM
(Marijo Volarevic, Vice President, Business Services)
13:00-14:00 Lunch
14:00-15:00 Questions & Answers


PRICE INFORMATION

Participation, coffee break and lunch at events are FREE of charge, registration however is required. Event participants are responsible for the arrangement and payment of their own travel and accommodation.


LOCATION

Hotel ARISTOS - Cebini 33, Buzin, 10010 Zagreb, Croatia
Click to get directions


HOW TO REGISTER

Fill the Registration form bellow and click submitt button. For any further information please contact Ms. Maja Judez (Tel: +386 7 393 06 00) or send her an email.

This event is closed for registration.

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