How to master data management to get IDMP ready 

11:00 am - 12:00 pm EDT | 23 September 2020  | Online

Catch the latest updates from our regulatory affairs experts, on the European Medicines Agency’s announcement for improved compliance on IDMP.

Amplexor and Genpact’s regulatory affairs experts are joining forces to present to you a webinar on IDMP compliance, and finding a suitable partner to make sure you are following the necessary steps to ensure proper data processing.

The European Medicines Agency has announced that by 2022, IDMP submissions will be compulsory, which means that data management will gain even more importance. This new rule will not only ensure that you are compliant, but will create better opportunities for data management, by going from paper to data-driven decisions and focusing more on quality and governance.  

Why attend?

  •  To learn how to handles issues such as data quality and governance 
  • To make the right choice for you in terms of technology selection 
  • To help guide your organization in seeing that IDMP is more than just about compliance

Meet the Speakers

David Gwyn

VP Life Sciences Solutions, Amplexor

With more than 25 years of experience in the Life Sciences industry, David Gwyn is a seasoned executive with extensive experience. As a Vice President for AMPLEXOR Life Sciences, David’s main focus is aligning customer needs with the capabilities of the company’s Life Sciences Suite to ensure that the solution meets the needs of the customer.


How to master data management to get IDMP ready

For more information and registration, please visit Genpact's website!