Parliamentary panel recommends bringing of CDSCO under Dept of Pharmaceuticals
Parliamentary panel attached to the Ministry of Chemicals and Fertilisers has asked the Ministry to check on quality of drugs.
Parliamentary panel attached to the Ministry of Chemicals and Fertilisers has asked the Ministry to take up urgently the matter of bringing the Central Drugs Standard Control Organisation (CDSCO) under the administrative purview of the Department of Pharmaceuticals for better check on quality of drugs.
Bringing back the contentious issue into focus, the standing committee headed by Gopinath Munde said the monitoring the quality of drugs and check on spurious drugs are interlinked with pricing and availability of drugs.
“The Department of Pharmaceuticals (DoP) may not be able to do full justice to its role regarding pricing and availability of drugs if the quality control set up does not come within its purview. The Committee, therefore, desire that the DoP should take up the matter regarding bringing the quality control and regulatory mechanism under one umbrella i.e. the DoP,” according to a recent report.
The debate has been going on for some time now over the issue. The DoP itself had taken up the matter with the Cabinet secretariat and the Prime Minister’s Office, clearly stating that the CDSCO may be brought under the DoP.
Pushing the matter to the PMO, Lok Sabha member Dr Sujan Chakraborty had also written to the Prime Minister some time back with the same demand. He pointed out that the very creation of the DoP was to bring all important functions under the single Department to facilitate growth of pharma industry. If the CDSCO was not brought under DoP, the very purpose of the DoP would remain unfulfilled, he said.
The DoP, in its submission to the PMO, also claimed that as the issues relating to pricing, availability and quality of medicines are closely interlinked, CDSCO should be a part of the DoP so that it may be able to play its role more effectively to achieve its main objective to ensure availability of life saving drugs at, reasonable prices as envisaged in the drug policy.
“Quality is an essential parameter while considering the pricing and availability of medicines. In the absence of jurisdiction over the issue of quality of medicines, the DoP finds itself handicapped to do full justice to the role assigned to it. It is, therefore, extremely important to bring the quality control set up under the DoP,” the department conveyed to the PMO.
“Since the function of price control and the administrative control of National Pharmaceutical Pricing Authority (NPPA) is already vested with the Department, this Department would be well equipped to address the significant issues related to the Pharmaceuticals,” it said.
Related News
-
News Panaxia's medical cannabis facility in Malta gains EU-GMP standard
This second facility gives the company a significant power multiplier for export capacity and geographical reach -
News CPhI Discover: Remote excipient audits are on the increase, but we must do more to develop novel excipients
Ahead of the session, Value Added Excipients to Unlock the Potential of APIs, at CPhI Discover on Thursday 18th May – global pharma’s largest ever virtual gathering – we spoke with one of the speakers, Dr Iain Moor... -
News Pharma Explained: What is Quality Risk Management & cGMPs?
Need clarity on determining your QA from your QbD and your cGMPs? You’re not alone! In our new Pharma Explained series from CPhI, we bring you clear cut definitions from industry experts on a myriad of Pharma Terms, delivered in bitesize video presenta... -
News Former FDA Commissioner lays out roadmap for building out excess capacity to deal with pandemic situations
Dr Scott Gottlieb shares insights into COVID-19 vaccine development, the upcoming US election and pharma pricing at the CPhI Festival of Pharma -
News Successful MHRA regulatory inspection for Scottish CMO Symbiosis
Inspection conducted remotely using video-conferencing and an online private document sharing platform. -
News Mylan and development partner win significant EPO ruling related to Copaxone
Decision clears legal pathway to expand access for patients living with multiple sclerosis in markets across Europe. -
News COVID-19 ushers in age of digital, flexible EU pharmaceutical regulation
The pandemic that has swept over the world in 2020 has caused huge disruption to the European pharmaceutical industry's regulatory procedures and supply chain management. But the crisis has also provided a platform for a learning process for the sy... -
News Europe's CHMP recommends suspension of medicines tested by Panexcell over flawed studies
The European Medicines Agency's human medicines committee (CHMP) has recommended the suspension of European marketing authorizations of generic medicines tested by Panexcell Clinical Laboratories at its site in Mumbai, India, citing irregularities in h...
Position your company at the heart of the global Pharma industry with a CPhI Online membership
-
Your products and solutions visible to thousands of visitors within the largest Pharma marketplace
-
Generate high-quality, engaged leads for your business, all year round
-
Promote your business as the industry’s thought-leader by hosting your reports, brochures and videos within your profile
-
Your company’s profile boosted at all participating CPhI events
-
An easy-to-use platform with a detailed dashboard showing your leads and performance