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Understanding How to Properly Evaluate Suppliers per FDA Requirements 21 CFR 820.50

Understanding How to Properly Evaluate Suppliers per FDA Requirements 21 CFR 820.50

Purchasing Controls and Supplier Evaluations are a critical component of quality management for medical device manufacturers, ensuring that materials,…

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Small Business Determination Requests Now Accepted Through CDRH Portal

Small Business Determination Requests Now Accepted Through CDRH Portal

The FDA recently released a significant update to its Center for Devices and Radiological Health (CDRH) Portal, allowing medical device companies to send…

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FDA Draft Guidance on Chemical Analysis for Biocompatibility Assessment of Medical Devices

FDA Draft Guidance on Chemical Analysis for Biocompatibility Assessment of Medical Devices

The FDA recently released a 45-page draft guidance detailing the use of chemical analysis in biocompatibility assessments for medical devices. This…

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We began as a small group of tech enthusiasts with a shared vision: to revolutionize the digital landscape. Over the years, we have grown into a full-fledged web design

9.05.2019

Importance of Software Testing on Software as Medical Device (SaMD)

MDR / 30.04.2019

8 Questions about the European MDR Answered

9.04.2019

FDA’s take on Digital Health Regulatory Paradigm Shift

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