Feb 24, 2022   |  GoToWebinar

Exploring the challenges and benefits of product data management across Regulatory, Safety, and Supply Chain

The implementation of Identification of Medicinal Products (IDMP) in the EU is driving efforts towards structured data submissions and digitization of product information. The upcoming requirement has significant impact to data management and surrounding business processes in the Life Sciences industry.

Although driven as a Regulatory requirement, there is significant global impact and overlap with initiatives in Pharmacovigilance and Serialization. There are also significant potential benefits as well.

Unfortunately, many companies operate with these functions in silos – partly due to the different pace that the requirements are being rolled out in different areas. This causes problems with data consistency and master data management, and limits the potential benefits of standardization. This webinar will discuss the similarities and differences in product tracking requirements across Regulatory, Pharmacovigilance, and Serialization, and will provide insights in to how you can best kickstart a master data strategy, and attain both tactical and strategic advantage.

Key Points:

  • Implementation of IDMP in the EU and the rationales behind it
  • Overlaps in product identification and requirements across Regulatory, Pharmacovigilance, and Serialization
  • The future of product identification and the impact to industry

Speakers:

  • Katherine Novak, Advanced Consultant, Life Sciences, NNIT
  • Mark Loudon, Advisory Director, Life Sciences, NNIT
  • Christoph Krähenbühl, Senior Director, Excellis Health Solutions – An NNIT Group Company

Register Now