- email:registrations@informa-ls.com
- phone:+44(0)20 7017 7481
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Regulatory Information Management
17 - 18 April 2012
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Regulatory Information Management
Regulatory Information Management: Only-of-a-kind in Europe
Informa Life Sciences’ 2nd annual conference on Regulatory Information Management addresses key topics to ensure that your regulatory processes are efficient and compliant.
SESSION HIGHLIGHTS
- Discover the latest industry progress with EVMPD... read more
- Understand the business drivers for regulatory information management... read more
- Gain practical advice on improving HQ-Affiliate communication and productivity... read more
- Hear and discuss practical and strategic insights on different RIM models... read more
- Examine real industry strategies and case study examples for centralised and decentralised data entry RIM models... read more
- Discuss essential considerations for RIM migration... read more
- New presentation topics on the agenda... read more
EVMPD Conference Exclusive...
Join industry experts and peers as they share the latest progress, experience and challenges in achieving compliance by 2 July 2012.
Click here for more information
New workshop leader
Huib van Ochten, Regulatory Affairs Manager at AstraZeneca in the Netherlands joins Andrey Mladenov to lead the pre-conference workshop!
EXPERT SPEAKER PANEL
EXPERT SPEAKER PANEL
Andrew Marr
Managing Director
Marr Consultancy
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Raun Kupiec
Senior Director, Regulatory Affairs Europe, Process Management Group
Genzyme
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Gursharan Moonga
Director
BritHealth Limited
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Gergely Zajzon
Director Business Development
AccepTher
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Event Sponsors
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What's new for 2012?
- 14 new speakers
- 1 whole session on EVMPD and IDMP!
- 17 new topics
- 6 new sessions on the agenda
- No streams - Don't miss a thing!
- No reduction in the number of presentations
INTERACTIVE SESSIONS
PRE-CONFERENCE WORKSHOP
How to set-up and implement a Regulatory Information Management project
Full workshop details
EVENING SEMINAR
Building the business case for a regulatory information management system
Full workshop details
SESSIONS OVERVIEW
Featuring an esteemed panel of senior-level regulatory affairs and operations professionals, you will take away practical advice and key messages in the areas of:
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Regulatory Information Management in practice
- Communication and information flow between affiliate and headquarter
- Managing RIM systems during mergers, acquisitions and in/out licensing
- EVMPD compliance and preparation for IDMP
- Regulatory Information Management data entry models
- Planning and tracking efficiencies
- Validation and archiving
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DATES AND VENUE
17 Apr 2012 - 18 Apr 2012
Radisson Blu Hotel, Berlin
Latest tweets
New sponsor confirmed!
We are delighted to welcome QUMAS as our welcome pack stationary sponsor.
SPONSORSHIP OPPORTUNITIES
Get great exporure by supporting one of the following:
Day 1 Evening Networking Drinks Reception (CSC confirmed)
Sponsored Lunch (Available)
Please click here for details
WHO SHOULD ATTEND?
Heads of Department, Directors, Managers, Team Leaders, Consultants and Coordinators from:
- Regulatory Affairs
- Global Drug Regulatory Affairs
- International Regulatory Affairs
- Worldwide Regulatory Affairs
- Regulatory Operations
- Regulatory Information/Data Management
- Regulatory Information Systems
- Systems Engineering
- Registration
- International Strategy
- Business Development
