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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Cybersecurity Post-Market Surveillance
Source:MEDIcept
Published on 2024-10-28
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Source:MEDIcept
Published on 2024-10-24
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Threat Modeling for Medical Devices
Source:MEDIcept
Published on 2024-10-21
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Securing Your Medical Device Software Development Life Cycle
Source:MEDIcept
Published on 2024-10-15
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What Makes a Great Clinical Research Associate? Site and Sponsor Perspectives
Source:MEDIcept
Published on 2024-10-07