One of the biggest challenges we are facing from our country Health Authority is to have "Separate Law Act for segregating Medical Devices, IVDs from Pharmaceutical Drugs as per Drugs & Cosmetics Act 1940 (India)." I would love feedback from my RAPS colleagues on what Regulatory challenges you have faced/are facing from your country Health Authority and what have you done to resolve those challenges?
Thank you!
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Gaurav Kumar
New Delhi
India
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