{"id":11137,"date":"2021-11-23T08:59:00","date_gmt":"2021-11-23T03:29:00","guid":{"rendered":"https:\/\/i3tk.org\/demo2\/?p=11137"},"modified":"2021-11-23T08:59:03","modified_gmt":"2021-11-23T03:29:03","slug":"national-digital-drugs-databank-will-help-address-information-asymmetry-in-pharma-space-cci-study","status":"publish","type":"post","link":"https:\/\/i3tk.org\/demo2\/world-news\/resources\/national-digital-drugs-databank-will-help-address-information-asymmetry-in-pharma-space-cci-study\/","title":{"rendered":"National digital drugs databank will help address &#8216;information asymmetry&#8217; in pharma space: CCI study"},"content":{"rendered":"\n<p>A national digital drugs databank will help in addressing &#8220;information asymmetry&#8221; as well as<br>provide key inputs in mapping the regulatory needs of different states, according to a<br>pharmaceutical sector study conducted by the Competition Commission of India. The fair<br>trade watchdog, which works on ways to foster competition and curb anti-competitive<br>practices, in the market study found that brand competition overrides price competition in the<br>domestic market where generic formulations are marketed with distinct brand names.<\/p>\n\n\n\n<p>Generic drugs play an important role in bringing down drug prices, thereby reducing<br>healthcare costs and improving access. In India, generics dominate pharmaceutical sales,<br>and the generic manufacturing within each molecule\/formulation market is characterised by<br>the presence of multiple manufacturers.<\/p>\n\n\n\n<p>The Competition Commission of India (CCI) has pitched for a multi-pronged and harmonised<br>regulatory response to the issue of drug quality, including setting up a national digital drugs<br>database.<\/p>\n\n\n\n<p>&#8220;A comprehensive, online, centralised drug databank consolidating real-time data on active<br>pharmaceutical manufacturing companies in the country, therapeutic class wise\/formulationwise approved branded\/unbranded products along with their manufacturing and marketing entities may be created, maintained, and made accessible to regulators, industry, physicians and consumers,&#8221; it noted.<\/p>\n\n\n\n<p>Such a database, the watchdog said, will help address information asymmetry and provide<br>important inputs in mapping the regulatory needs in different states.<\/p>\n\n\n\n<p>Information gaps on grant of licences, inspections and prosecutions for non-compliance,<br>among others, could be bridged through real-time data that could be published on a central<br>online portal, it added.<\/p>\n\n\n\n<p>As per the study released on Thursday, a pre-requisite for competition in generics to move<br>from non-price to price dimension is to dispel concerns about drug quality.<br>Promotion\/ facilitation of generic entry, prescription by generic drug name and substitution<br>between generics by chemists, which are reckoned as vital pro-competitive instruments, can<br>yield the desired outcome of exposing pharmaceutical expenditure to significant price<br>competition, subject to certain conditions.<\/p>\n\n\n\n<p>&#8220;\u2026only when all generic drugs in a therapeutic class in their unbranded and branded versions<br>are considered interchangeable and equally efficacious by stakeholders,&#8221; the study noted.<\/p>\n\n\n\n<p>Another suggestion is to have an institutional quality-signalling mechanism through the<br>printing of standard compliance marks on unbranded drugs, which meet the quality<br>standards.<\/p>\n\n\n\n<p>&#8220;This may provide the necessary confidence to the physician community to prescribe generic<br>names. This can also boost consumer confidence in unbranded generic drugs,&#8221; the study<br>said.<\/p>\n\n\n\n<p>Uniform and effective implementation of existing quality standards, better transparency,<br>quality control across the supply chain as well as in public procurement are among the other<br>suggestions.<\/p>\n\n\n\n<p>About online pharmacies, the study said such entities should adopt self-regulatory measures<br>in the areas of collection, use, sharing of data and privacy.<\/p>\n\n\n\n<p>&#8220;However, for safeguarding patient privacy and protecting sensitive personal medical data,<br>necessary regulations need to be enforced until the country legislates its data protection law,&#8221;<br>it added.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>In India, generics dominate pharmaceutical sales, and the generic manufacturing within each molecule\/formulation market is characterised by the presence of multiple manufacturers.<\/p>\n","protected":false},"author":1,"featured_media":10291,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[87],"tags":[],"class_list":["post-11137","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-resources"],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v18.8 (Yoast SEO v27.4) - https:\/\/yoast.com\/product\/yoast-seo-premium-wordpress\/ -->\n<title>National digital drugs databank will help address &#039;information asymmetry&#039; 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