Free Distribution of Life Saving and Generic Medicines: Minister Reply

Published On 2016-12-27 06:06 GMT   |   Update On 2016-12-27 06:06 GMT

Following is the written reply given by Minister of State (Health and Family Welfare), Sh Faggan Singh Kulaste to Lok Sabha on the issue of Free Distribution of Life Saving and Generic Medicines .


Public health being a state subject, it is for the States/UTs to draw up such action plans as per their need. Under the National Health Mission (NHM), financial and technical support is provided to the States/UTs for strengthening their healthcare delivery system including support for provision of essential drugs free of cost to those who access public health facilities. An incentive of upto 5% additional funding (over and above the normal allocation of the state) under the NHM is provided to those states that effectively implement free essential medicines initiative. All the States/UTs have reported that they have notified free drug policy in their respective States/UTs.


The National Free Drugs Service Initiative under the National Health Mission does not specify the number of essential drugs to be provided free of cost. Public health being a State subject, the number of essential drugs to be provided free of cost is decided by the States and varies from State to State. However, the Ministry has provided illustrative list of essential medicines that should be provided at Sub Centres, Primary Health Centres, Community Health Centres and District Hospitals.


The steps taken by the Government to check Spurious/Sub-Standard Drugs in the country include:


· Amending the Drugs and Cosmetics Act, 1940 by the Drugs & Cosmetics (Amendment) Act, 2008 to provide for more stringent penalties for manufacture and trade of spurious and adulterated drugs.


· Making provisions in the Drugs & Cosmetics (Amendment) Act, 2008 for setting up of Special designated courts for speedy disposal of cases to deal with the cases of offences under the Drugs and Cosmetics Act.


· Issuance of guidelines for taking action on samples of drugs declared spurious or not of standard quality in the light of enhanced penalties under the Drugs & Cosmetics (Amendment) Act, 2008 on the Website of CDSCO for purpose of uniform implementation of Drugs and Cosmetics Act in the Country.


· Initiation of Whistle Blower Scheme to encourage vigilant Public Participation in the direction of Movement of spurious drugs in the country.


· Providing assistance for upgrading of testing facilities and establishing new drug testing laboratories under the Capacity Building project through Wold Bank, so as to enhance the capacity of the laboratories to test large number of samples.


· Overseas inspection of drug manufacturing sites to ensure quality of imported bulk drugs.


· Amendment of Schedule m to the Drugs and Cosmetics Rules, 1945, pertaining to Good Manufacturing Practices in 2001 to make it at par with the international standards. It is mandatory for the manufacturers of drugs to comply with requirements of this schedule for quality control of the drugs manufactured by them.


· Introduction of Good laboratory Practices.


· States have been advised to incorporate adequate quality assurance safeguards while procuring drugs.


Article Source : Press release

Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News