According to Gartner April 2022 Market Guide for Life Science Regulatory Information Management Solutions report, we’re a Representative Vendor.
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, companies must find ways to maximize return on investment by manufacturing products as efficiently and cost-effectively as possible.
To serve global markets, they must produce 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.
Read this eBook to learn about:
- The value of a Regulatory Information Management (RIM) system
- The evolution of RIM
- The imperative of RIM and why it matters NOW
- The benefits of RIM
Disclaimer: Gartner Market Guide for Life Science Regulatory Information Management Solutions, Rohan Sinha and Jeff Smith, 4 April, 2022.
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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.