The Need for Better Regulatory Information Management in Medical Device Manufacturing

Webinar with xTalks

Medical device companies face an extraordinary set of challenges today. Complex and constantly changing regulatory compliance, growing product quality requirements and the evolving landscape of digital technologies are both an opportunity and a challenge for medical device companies seeking to compete and innovate.

To navigate this environment, they must develop products that comply with global regulations, adhere to each country’s submission process and meet growing customer needs — and they must do all this in a timely manner.

View this webinar and learn actionable insights around the following areas:

  • Regulatory information management strategies
  • Technology approach to better manage and structure internal teams, processes and data
  • Preparing your organization to better navigate future regulatory and organizational changes like EU MDR, UDI and others


Speakers

Caroline Byrd
Caroline Byrd
Director, Commercial RAQA Leica Biosystems
Van Gresham 2015
Van Gresham
Partner Kalypso
Ian Bennett
Ian Bennett
IT Transformation, Sr. Manager Smith & Nephew
Rich Randall
Rich Randall
Solution Architect, PLM Processes Kalypso