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Veeva Global Regulatory Transformation for Medical Devices

Wednesday, Dec 11, 2019

Are You Ready for the MDR Enforcement Deadline?

Medical device companies are transforming the way they manage regulatory information and operations to comply with the new requirements of MDR. Join RAPS and Veeva for a 60-minute live webcast of a fireside chat with Lori Holder, the director of regulatory affairs at Alcon. She and Veeva will discuss how the Alcon team is unifying regulatory operations to create a sustainable operating model for the future.

Fireside Chat: Alcon Discusses Global Regulatory
Transformation for Medical Devices

Wednesday, 11 December 2019
10:00 – 11:00 am MT
1.0 RAC Credit

This intermediate-level webcast is designed for:

  • Employees of medical device companies preparing management and operations to meet the new MDR requirements
  • Employees of pharma, medical device and diagnostics companies that are interested in learning more about a unified RIM solution
  • Regulatory professionals involved with compliance and audits
  • Regulatory professionals managing global regulatory intelligence

Register here.