List of National Regulatory Authorities (NRAs) operating at maturity ...

List of National Regulatory Authorities (NRAs) operating at maturity level 3 (ML3) and maturity level 4 (ML4) - Select language - العربية 中文 français русский español português (as benchmarked against WHO Global Benchmarking Tool (GBT) (in alphabetical order)

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List of National Regulatory Authorities (NRAs) operating at maturity ...

Tanzania Medicines and Medical Devices Authority (TMDA) ML3 1. Medicines 2. Vaccines (non producing) 2018 Viet Nam Vaccine regulatory system in Vietnam represented by: a) The Drug Administration of Viet Nam (DAV), b) Administration of Science, Technology and Training (ASTT), c) National Institute for the Control of Vaccines and

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List of stringent regulatory authorities - Wikipedia

A stringent regulatory authority (SRA) is a national drug regulation authority which the World Health Organization (WHO) considers to apply stringent standards for quality, safety, and efficacy in its process of regulatory review of drugs and vaccines for marketing authorization. [1]

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List of Regulatory Authorities

List of Drug Regulatory Authorities of Different Countries. Asia. 1. India - The Central Drugs Standard Control Organisation(CDSCO) 2. Pakistan - Drug Regulatory Authority Of Pakistan. 3. China - The National Medical Products Administration (NMPA) 4. Malaysia - National Pharmaceutical Regulatory Agency (NPRA) 5.

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National competent authorities (human) - European Medicines Agency (EMA)

A list of competent authorities of the Member States responsible for the authorisation of medicinal products for human use at national level and/or for the authorisation of clinical trials is provided below. For more information on how EMA works together with the national competent authorities, see European medicines regulatory network.

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operating at maturity level 3 (ML3)1 2 (as benchmarked against WHO ...

List of National Regulatory Authorities (NRAs) operating at maturity level 3 (ML3) ... As of April 2022 Country Regulatory authority Maturity Level (ML) Scope of products Year of announcement Egypt Egyptian Drug Authority (EDA) ML3 1. Vaccines (producing) 2022 Ghana Food and Drugs Authority (FDA) ML3 1. Medicines

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Regulatory Authorities worldwide - an overview list - EXTEDO

Are you familiar with the Regulatory Authorities worldwide? With the ever-changing regulatory landscape, it is important for companies in the life sciences to stay informed and up to date with the latest developments around the world. For this reason, we created an overview of all Regulatory Authorities worldwide in the life sciences.

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National regulatory authorities (NRAs) | www.acer.europa.eu

National regulatory authorities (NRAs) have a key role to play in ensuring that each European country meets its targets for energy markets and implements the relevant EU regulatory policy.. In order to maintain the proper functioning of the single European market in gas and electricity, ACER supports NRAs in performing their regulatory function at European level and coordinates their ...

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WHO Expands List of Trusted Regulatory Agencies to 36, including US FDA ...

WHO has expanded its list of trusted national regulatory authorities from three to 36 agencies – including the United States Food and Drug Adminstration (FDA), the European Medicines Agency (EMA) as well as the European Medicines Regulatory Network (EMRN), composed of the European Commission, and thirty national regulatory agencies.

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Global Regulatory Authority Websites - PDA

National Health Authorities (by Region) Asia and the Pacific. Australian Government: Department of Health and Ageing Australian Government: Therapeutic Goods Administration Brunei: Ministry of Health People's Republic of China People’s Republic of China: National Medical Products Administration People's Republic of China: Ministry of Agriculture

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List of stringent regulatory authorities

A stringent regulatory authority (SRA) is a national drug regulation authority which the World Health Organization (WHO) considers to apply stringent standards for quality, safety, and efficacy in its process of regulatory review of drugs and vaccines for marketing authorization.

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