How To Do a Medical Device Risk Management

Diagnostic and treatment of patients are done using multiple medical devices. It is a complex task for researchers to create medical devices that are effective yet safe for human use. Risk management is the process of identifying hazards and risk control. It is about identifying, analyzing, controlling, and preventing device failures that can cause hazards.

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4 Common Medical Device Compliance Problems

Effective planning helps you get success in the medical device manufacturing industry. Unfortunately, the industry has seen many high-profile medical regulatory compliance issues. Luckily, looking at their mistakes, you can learn to have better medical device and equipment compliance. In this article, we are listing the four most common medical regulatory compliance issues. These issues

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FDA’s New Social Media Policy

The social media policy of FDA applies to all employees and contractors of the drug administration. The policy outlines expectations and guidelines to encourage healthy use of technologies that support FDA’s communication and exchange of credible information with the primary interest of protecting and promoting public health. Definition and scope of the policy FDA defines

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