Last Updated on October 10, 2024 by The Health Master
The Indian Pharmacopoeia Commission (IPC) will be organizing a webinar on “Key role of medical technology / medical device industries in Materiovigilance Programme of India’ (MvPI) in association of Central Drugs Standard Control Organisation (CDSCO) and Association of Indian Medical Device Industry (AiMeD) on December 10, 2021.
The speakers include:
- Dr V G Somani, Drugs Controller General of India (DCGI) , CDSCO,
- Rajiv Nath, forum coordinator, AiMeD,
- Dr Jitendra Sharma, CEO, Andhra Pradesh Med Tech Zone,
- Rajeev Singh Raghuvanshi, secretary-cum-scientific Director, IPC
- Dr. Vivekanandan Kalaiselvan, Senior Principal Scientific Officer, IPC.
This webinar will sensitize the manufacturers, importers, distributors of medical devices, including all healthcare stakeholders across India in order to promoting the patient safety and strengthening of materiovigilance system in India.
The manufacturers, distributors, importers, regulators of medical devices, healthcare professionals and researchers can attend this webinar.
The expected outcome of this webinar is to stimulate the culture of adverse event reporting associated with medical devices and the strengthening of an effective materiovigilance system across the country.
The registration fees is Rs.1,000 (including 18% GST) per participant.
AiMeD is an umbrella association of Indian Manufacturers of Medical Devices covering all types of medical devices, including consumables, disposables, equipments, instruments, electronics, diagnostics and implants.
Materiovigilance Programme of India has the responsibility to monitor, collate, and analyse the adverse events associated with the use of medical devices in the Indian population.
The vision of IPC is to promote the highest standards of drugs for use in human and animals within practical limits of the technologies available for manufacture and analysis.
IPC is an autonomous institution of the ministry of health and family welfare, Government of India.
IPC is created to set standards of drugs in the country. Its basic function is to update regularly the standards of drugs commonly required for treatment of diseases prevailing in this region.
The mandate of the commission is to perform, inter-alia, functions such as revision and publication of the Indian Pharmacopoeia and National Formulary of India on a regular basis besides providing IP reference substances and training to the stakeholders on pharmacopoeial issues.
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