Are You Preparing for the Medical Device Single Audit Program (MDSAP) Audit Process?
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Are You Preparing for the Medical Device Single Audit Program (MDSAP) Audit Process? Read More »
Here is the blog for every IVD manufacturers to know about the IVD regulatory framework to improve the health and safety of patients and users.The utilization of the term \’in vitro\’, which in Latin signifies \’in glass\’, is an impression of the way that most by far of these tests were initially performed in a test tube.
Why IVD Regulation Framework Is Done Separately? Read More »
The ultimate guide for Ethiopia medical device registration by FMHCACA (Food, Medicine, and Health Care Administration and Control Authority). Learn more about the medical device and IVD\’s classification and approval process for Ethiopia.
Ethiopia Medical device registration | Ethiopian Regulation Read More »
For Medical Device Registration In South Africa, the South African government has established a new agency to manage the new medical device and pharmaceutical regulatory systems being produced in the country.
Medical Device Registration In South Africa Read More »
This is the most comprehensive guide for every manufacturer who wants to the medical device registration in different countries all around the globe.Let’s check QMS certification for different countries all over the globe which helps you to market your product globally.
Guide for Medical Device Regulations by Countries Read More »