Regulatory Consulting Services
• Medical Device • In vitro Diagnostics • Cosmetics • Pharmaceuticals
MEDICAL DEVICES
As medical device regulatory affairs professionals, it can be challenging to stay on top of changes happening in our industry. Few people have the time to read lengthy articles these days and although many online newsletters exist, they are often packed with PR releases, ads or unrelated information. That is why we started this blog for RA professionals in the medical device and IVD industry. The idea is to give you short updates on regulatory topics that may be of interest to you. Without manufacturing of medical device we can also sell products within India, they need to be in compliance with India’s minimal medical device regulations. India publishes a list of devices on the basis of the classification that require registration. The registration of these products is regulated under the provisions of