There are many reasons why life sciences companies should not delay their data-driven regulatory information management initiatives.

At his session during Amplexor’s BE THE EXPERT on 28 May, Frits Stulp of Iperion Life Sciences Consultancy spelled out the accelerating urgency around data-driven transformation of regulated information processes, provided an update on the latest status of IDMP, and explored the shift towards electronic product information as one of the latest use cases that will invite change.

Watch the webinar on demand

Webinar

Amplexor’s BE THE EXPERT 2020 brings together leading subject matter experts and industry professionals from around the world into one forum to discuss and exchange strategies that combat the challenges in an ever-changing regulatory landscape. You will walk away with enhanced knowledge that will position you to achieve positive results and transform the processes and technology within your business environment.

Hosted by Frits Stulp

Frits is Managing Director of Iperion Life Sciences Consultancy and IDMP SME. He has 18+ years of experience within the Life sciences industry. As a project manager he is specialized in management of IT projects for Regulatory Compliance, and has been the Program Manager of the first completed IDMP implementation program. Frits supports several clients as IDMP program advisor. Frits been a member of the EMA ISO IDMP Task Force and is an active speaker on IDMP on conferences and webinars.

If you have any questions on IDMP implementation or want support in implementing, please contact us.

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