Welcome to RIMtelligence, Instem’s new bi-weekly blog. We are excited to develop an online community where regulatory professionals can follow our subject matter experts to read and share insights about some of the most important matters facing all of us today. From regulatory updates and compliance, to learning about trends for streamlining processes to increasing efficiencies, we hope this becomes a regular destination for you.
Meeting with clients and prospects around the world, we know the specific challenges the Medical Device industry is faced with – unprecedented change, driven by the need for technology innovation amidst a rapidly-evolving, global regulatory framework.
We believe that Instem is uniquely positioned and look forward to offer insight and expert opinions to help you navigate the new and ever-changing regulatory environment.
Look for blog posts from us every other Thursday. And, reach out if you have any suggestions for content or want to comment on the current topic. You can email Kim Young, Instem’s Regulatory Intelligence subject matter expert and RIMtelligence’s primary author, at firstname.lastname@example.org.
While we have your attention, join us for a TOPRA Course-Webcast on Wednesday, April 22nd to learn how to ensure sustained compliance with the EU-MDR and IVDR utilizing end-to-end technology operations automation. More information can be found here: https://bit.ly/3b57o6y.