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
Disclaimer: Gartner Market Guide for Life Science Regulatory Information Management Solutions, Jeff Smith, 11 December, 2020.
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GARTNER is a registered trademark and service mark of Gartner, Inc. and/or its affiliates in the U.S. and internationally and is used herein with permission. All rights reserved.
Gartner does not endorse any vendor, product or service depicted in its research publications, and does not advise technology users to select only those vendors with the highest ratings or other designation. Gartner research publications consist of the opinions of Gartner’s research organization and should not be construed as statements of fact. Gartner disclaims all warranties, expressed or implied, with respect to this research, including any warranties of merchantability or fitness for a particular purpose.
GARTNER is a registered trademark and service mark of Gartner, Inc. and/or its affiliates in the U.S. and internationally and is used herein with permission. All rights reserved.