MEDIcept
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.
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Jason Gromek Appointed as MEDIcept President and CEO
Source:MEDIcept
Published on 2025-03-17
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High-Risk IVDs Drive Immediate Transition to IVDR
Source:MEDIcept
Published on 2025-03-11
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Top 5 Upcoming FDA and EU Regulations – What to Know for 2025
Source:MEDIcept
Published on 2025-01-13
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Selecting the Right EDC for your Clinical Trial: The Difference in Device Approval
Source:MEDIcept
Published on 2024-11-26
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Source:MEDIcept
Published on 2024-11-22
