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Expert Review of Clinical Pharmacology Volume 14, 2021 - Issue 2

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Reliance: a smarter way of regulating medical products - The IPRP survey

Petra Doerra Regulation and Safety Unit, World Health Organisation, Geneva, SwitzerlandView further author information

Marie Valentina Regulation and Safety Unit, World Health Organisation, Geneva, SwitzerlandCorrespondence[email protected]
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Nobumasa Nakashimab Pharmaceuticals and Medical Devices Agency, Tokyo, JapanView further author information

Nick Orphanosc Health Canada, Ottawa, CanadaView further author information

Gustavo Santosd ANVISA, Brasília, BrazilView further author information

Georgios Balkamose European Commission, Brussels, BelgiumView further author information

Agnes Saint-Raymondf European Medicines Agency, Amsterdam, NetherlandsView further author information

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Pages 173-177 | Received 04 Sep 2020, Accepted 15 Dec 2020, Published online: 23 Dec 2020

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https://doi.org/10.1080/17512433.2021.1865798
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World Health Organization. WHO good reliance practices. [ cited 2020 Dec 2]. Available from: https://www.who.int/medicines/areas/quality_safety/quality_assurance/QAS20_851_Rev_1_Good_Reliance_Practices.pdf?ua=1
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International pharmaceutical regulators programme. [cited 2020 Dec 2]. Available from: www.iprp.global
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International Pharmaceutical Regulators Programme. IPRP reliance survey. [cited 2020 Dec 2]. Available from: http://www.iprp.global/news/outcome-who-survey-reliance
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World Health Organization. WHO global benchmarking tool. [cited 2020 Dec 2]. Available from: https://www.who.int/medicines/regulation/benchmarking_tool_version_vi/en/
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World Health Organization. WHO draft policy on evaluating and publicly designating regulatory authorities as WHO-listed authorities. 2019 [cited 2020 Dec 2]. Available from: www.who.int/medicines/areas/quality_safety/quality_assurance/QAS19_828_Policy_on_WHO_Listed_Authorities.pdf?ua=1
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