Archive Newsletter

  1. 03.25.21 -- The 6-Step Checklist For IVDR Compliance 3/25/2021
    03/25/21 Med Device Online Newsletter
  2. 03.24.21 -- Addressing The Challenges Associated With The Development And Commercialization Of Combination Products 3/24/2021

    03/24/21 Med Device Online Newsletter

  3. 03.23.21 -- Statistics Abuse In QA/QC: 3 Lessons Learned 3/23/2021
    03/23/21 Med Device Online Newsletter
  4. 03.18.21 -- U.S. FDA And Medical Device Regulations In 2021 | Intro To Injection Mold Verification 3/18/2021
    03/18/21 Med Device Online Newsletter
  5. 03.16.21 -- Germany's Digital Medical Device Regulations: A Framework For The World To Follow, Part III 3/16/2021
    03/16/21 Med Device Online Newsletter
  6. 03.11.21 -- Answer These 3 Questions Before Developing Software As A Medical Device 3/11/2021
    03/11/21 Med Device Online Newsletter
  7. 03.10.21 -- Listen Now - The FDA's Progressive Appeal, AI And The Human Genome, And More 3/10/2021
    03/10/21 Med Device Online Newsletter
  8. 03.09.21 -- FDA's COVID-19 PREPP Initiative Summary Report -- Key Takeaways For Manufacturers 3/9/2021
    03/09/21 Med Device Online Newsletter
  9. 03.04.21 -- Risk Intelligence And Risk-Based Decision-Making | 7 Rules For Properly Interpreting Control Charts 3/4/2021
    03/04/21 Med Device Online Newsletter
  10. 03.02.21 -- Germany's Digital Medical Device Regulations: A Framework For The World To Follow, Part II 3/2/2021
    03/02/21 Med Device Online Newsletter