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Information Management and Data Quality for Pharma Sector
Berlin, Germany
20/11/2017 - 22/11/2017
URL:   Click here for the event website.
This marcus evans conference will focus on gathering corporate professionals from Regulatory Operations, Regulatory Affairs, Master Data Management, Regulatory Information Systems and other key stakeholder departments progressing on IDMP projects in the uncertainty context with already some lessons learnt and practices to share for those who are less advanced in the journey.

Attending this premier marcus evans conference will enable you to:
Turn IDMP into long term information management project
Realise IDMP benefits outside of compliance
Establish good data quality production and maintenance
Discuss good practices around structuring unstructured data
Manage effective compliance work and IDMP strategy in the uncertainty context

Expert Speakers Panel includes:
Dr. Andrea Herrmann, MDRA, Director, Strategy Implementation Leader Biopharma | R&D Strategy and Business Operations, Merck
Charlotte Ratcliffe, Regulatory Information Management, IDMP project, Grünenthal GmbH, Quentin Grignet, IDMP Lead, GSK Vaccines
Guido Claes, Director MDM for Pharma R&D, Janssen Pharmaceutical Companies of Johnson and Johnson
Dr. Andrew Marr, Internationally recognised IDMP Compliance Expert Member, Marr Consultancy Ltd

Special offers for CanBiotech members using code CS121-CB when registering for this event
2 day conference: -£200
2 day conference & 1 workshop: -£250
2 day conference & 2 workshops: -£350
(Not for solution providers and consultants)

Interested? If you feel that you are a good fit for this conference please visit the event website:

For more information simply send an email to
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