Featured Speakers :

 Andrew Marr
Andrew Marr
Managing Director
Marr Consultancy Ltd
 Susanne Koch
Susanne Koch
Head of Enterpriese Architecture
Boehringer-Ingelheim Pharma GmbH
Dr. Gerhard Noelken
Dr. Gerhard Noelken
Senior Director Technology & Innovations
Pfizer
Dr. Klaus Menges
Dr. Klaus Menges
Direktor
Bundesinstitut für Arzneimittel und Medizinprodukte
Dr. Jaroslava Paraskevova
Dr. Jaroslava Paraskevova
Head of Documentation Management & Information Service / eCTD
MEDA Pharma GmbH & Co. KG
Dr. Elke Schydlo
Dr. Elke Schydlo
Global Head Submissions & Registration Management
Mylen EPD
 Bodo R. V. Antonic
Bodo R. V. Antonic
Lehrbeauftragter und Studienleiter
HTW Aalen
Dr. Jean-Michel Cahen
Dr. Jean-Michel Cahen
IDMP Project Lead
Novartis Pharma S.A.S
Dr. Quentin Darrasse
Dr. Quentin Darrasse
Global Quality Manager for Regulatory Operations
F. Hoffmann-La Roche AG
Dr. Andreas Franken
Dr. Andreas Franken
Abteilungsleiter Klinische Forschung / elektronische Verfahren
Bundesverband der Arzneimittel-Hersteller e.V.
 Jose Falcon Hernandez
Jose Falcon Hernandez
Regulatory Affairs Leader
GE Healthcare
 Sue Metz
Sue Metz
Director (rim) Regulatory Intelligence
Parexel

IDMP Implementation - Impact on Data, Systems and Processes

How to cover gaps for IDMP implementation till July 1st 2016?

ISO IDMP will be mandatory from July 1st 2016 and it will make a fundamental impact on the way the pharmaceutical industry is required to collect, manage and submit relevant data. Now is the last call for all marketing authorisation holders to (re)think their data submission policies and processes to make sure you close your IDMP implementation gaps in the next 12 month and have a clear vision of the next challenges lying ahead!

Our conference is dedicated to support companies in better understanding, prioritizing and implementing strategies on the way into seamless and fully compliant regulatory information and content management.  

Don’t miss out on the opportunity to get your questions answered, to benchmark the stage of your preparation, to initiate partnerships and to take an active part in designing the RIM’s community future agenda! Join us this summer in Berlin and gain valuable, practical information:

  • Learn how to assess and analyse data requirements for the IDMP standards by discussing possible interpretations with our expert from regulatory bodies on-site!
  • Benchmark your own IDPM Implementation process with peers from both big and mid-size pharma
  • Share insights how the IDMP standards are changing the interactions between IT-Systems, company departments, contract manufacturers and regulatory agencies 
  • Discuss and compare with your peers experiences with vendors and solution providers offering help to achieve your IDMP implementation goals!

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