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MEDIcept

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Description

With decades of combined experience in medical device design and manufacturing and regulatory compliance, we are uniquely qualified to help medical device, in-vitro diagnostic, and plasma pharmaceutical companies navigate complex FDA and international regulatory pathways, reduce business risk and time-to-market while maximizing the potential for success in the market.

  • Strengthening Medical Device Security in the Age of AI Threats


    Source: MEDIcept


    Published on: 2025-08-12

  • Risk Management Series – Part 5: Assigning Harms and Severity


    Source: MEDIcept


    Published on: 2025-05-20

  • Risk Management Series – Part 4: Key Terms


    Source: MEDIcept


    Published on: 2025-04-16

  • Jason Gromek Appointed as MEDIcept President and CEO


    Source: MEDIcept


    Published on: 2025-03-17

  • High-Risk IVDs Drive Immediate Transition to IVDR


    Source: MEDIcept


    Published on: 2025-03-11

tax credits Regulatory submission Regulatory strategies medical device FDA
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200 Homer Ave, Ashland 01721, USA
123 *** *** 508-231-8842
Monday 9:00 AM - 6:00 PM
Tuesday 9:00 AM - 6:00 PM
Wednesday 9:00 AM - 6:00 PM
Thursday 9:00 AM - 6:00 PM
Friday 9:00 AM - 6:00 PM
Saturday Closed
Sunday Closed
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