All the manufactuers are advised to ensure compliance of provisions, otherwise they will be liable to deposit the overcharged amount with interest”.These devices are non-scheduled formulations and their sales are governed by the provisions of DPCO 2013, the notification said.. This is a blatant violation of law of the land, it added. The NPPA had recently announced major price cuts for cancer drugs, up to 86 per cent in some cases and reduced cardiac stent prices by over 75%, capping the ceiling prices of drug eluting stents and bioresorbable vascular scaffolds at Rs 29,600, and bare metal stents at Rs 7,260, including VAT, these stents are expected to cost Rs 31,080 and Rs 7,623, respectively. The prices of non-scheduled formulations are monitored by the government.”Sources said the notification was issued following complaints China Macaron Color Mask Company from the patients being charged exorbitant prices on these medical devices.New Delhi: After controlling prices of stents, India’s drug pricing regulator, National Pharmaceutical Pricing Authority , has made it mandatory for the manufacturers and importers of “notified” medical devices to carry maximum retail price on the packs. Manufacturers are not allowed to increase the price of these more than 10 per cent per annum, NPPA said.Sources said that the move is expected to bring transparency and relief to consumers who could otherwise be taken for a ride as their prices are neither monitored nor controlled. These devices include heart valves, catheters, bone cements, surgical dressings, condoms, stents, disposable hypodermic syringes, orthopaedic implants, intra ocular lenses, umbilical tapes, intra uterus devices among others. In its tweet, the NPPA said: “Total 22 medical devices notified as ‘drugs’ must print MRP on the packs under DPCO, 2013; state govts/state drug controllers requested to enforce law.“It has come to knowledge of the NPPA that several medical devices are available in the market and are also being used in healthcare facilities where no MRP is printed on the package by manufacturers/importers,” the NPPA said in a notification. The government has notified 22 medical devices as drugs under the Drugs and Cosmetics Act, 1940, and the Drugs and Cosmetic Rules, 1945, it said.

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