The new medical device rule “MDR 2017, India” has come into effect from January 2018. In line with that, the CDSCO (Central Drug Standard Control Organization) has recently been releasing guidance documents,
More In light of the new Medical Device Rules 2017, CDSCO/CLA/SLA shall have updated information of laboratories involved in testing of medical device & in vitro diagnostics with respect to their laboratory reports and decision on performance evaluation of products made by stakeholder/regulator.
More The Department of Industrial Policy and Promotion, Ministry of Commerce and Industry, Government of India has recently issued guidelines for implementation of Public Procurement Order No. 17 (PPO) in an aim to mandate procuring entities to make local suppliers as their priority purchase preference for medical devices,
More The Government of India, Ministry of Health and Family Welfare has released guidelines with respect to Grouping of Medical Devices for applicants who intend to apply for a license to import or manufacture medical devices for sale and distribution in India.
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The Government of India and the Ministry of Health and Welfare have issued guidelines for the grouping of medical devices on the wish to apply for a license to import or manufacture medical devices for sale and distribution in India.
More The Ministry of Industrial Policy and Promotion, the Ministry of Commerce and Industry, and the Indian government have recently issued Public Purchase Order No. 17 in order to force procurement entities to use local suppliers as the priority procurement preference for medical equipment, as well as other products and services related to the pharmaceutical sector. (PPO) guidelines.
More The Times of India reported on 21st of January 2018 about the two-day international conference on “'Challenges, opportunities and newer directions of pharmacovigilance and clinical research in India' sponsored by the All India Council for Technical Education (AICTE).
More India's central medical device regulator, the Central Drugs Standards Control Organization (CDSCO) published, on November 1, 2017, a revised risk classification of medical devices and IVDs on the basis of their intended use. This is an extremely important development for the medical device and IVD industry because from January 1, 2018 onwards,
More The Government of India notified in February 2017 the new Medical Device Rules 2017, which will come into force starting January 1, 2018. The new Rules have been framed in conformity with Global Harmonisation Task Force (GHTF) framework and conform to best international practices.
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