PharmD Info

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Find Quality Assurance - Guidelines and SOPs, Role of Quality Assurance in Pharmaceutical Industries and QA Discussion Forum.
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As per Medical Devices Rules 2017, medical devices are classified based on the followings;

1. Intended for medical use
2. Risk associated with the device

Updated list of medical devices placed at Appendix A

Download Here

Risk levels are classified as A, B, C, D based on its level of risks

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