Medical Device Vigilance

In the same way as pharmaceutical companies must monitor and report on adverse reactions to their medicinal products, manufacturers of medical devices are also required to report adverse incidents to competent authorities.

How can we help?

To support you through your medical device vigilance obligations, we can help you design vigilance and risk management systems for monitoring and controlling the risks associated with the use of medical devices by patients, users and others, as well as ensuring your processes comply with required Guidelines.

For a more detailed discussion on how we can help you, contact us on +91 886000 9879 or email us via our contact form

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