Eight proposed parks aim to reduce import dependence, boost local manufacturing
Making essential drugs easily available is important in a country like India, which has less than one doctor per 1,000 people
Health ministry has issued a draft notification to define all medical devices under Drugs and Cosmetics Act
The proposed body will be separate from the Central Drugs Control Standard Organisation, which will continue to be the regulator for drugs
This will be on the lines of the Drugs Technical Advisory Board (DTAB), which looks into issues in the pharmaceuticals sector
The growth in imports was led by product categories such as diagnostic items, ultra-sonogram machines, and more
A range of medical devices, old or new, will soon have an 'Indian standard' and nearly 1,000 products are presently being benchmarked, a top government official said Thursday. NITI Aayog member V K Paul, in his address at a conference here, said the standardisation is expected to be completed in the next two months. "We don't have any Indian standards (for medical devices). As we speak, about 1,000 products' standards are being completed, and the deadline for that is about two months from now. "And, from old devices to new, most of the important devices will carry Indian standardisation from the BIS," he said. The Bureau of Indian Standards (BIS) is the national standards body of India working under the aegis of the Ministry of Consumer Affairs, Food & Public Distribution. The conference MedTekon 2018 -- MedTech Vitalsing Ayushman Bharat, organised by Medical Technological Association of India (MTaI) was also attended by Swedish envoy Klas Molin. Molin said Sweden, both at ...
National Pharmaceutical Pricing Authority has begun collecting data from device makers
Pricing regulation on medical devices gains momentum
The government move to cap device prices is getting political attention too
Modi's government has in recent months slashed prices of medical devices such as knee implants and heart stents by up to 75 percent to make them more affordable.
Govt has notified 22 medical devices as drugs under Drugs and Cosmetics Act, 1940
Rules classifies medical devices in to 4 groups based on associated risks - Class A, B, C & D
Final regulations may not change from the draft despite industry protests
The new draft wants companies to specify manufacturing date along with expiry date on packaging
Medical devices to get licences within six months of notification
A report by Deloitte and NATHealth says global medical devices and technology market is expected to grow to $520 bn by 2020