The Challenges of Regulatory Pluralism

Author:

Gillner Sandra,Blankart Katharina Elisabeth,Bourgeois Florence Tanya,Stern Ariel Dora,Blankart Carl Rudolf

Publisher

Elsevier BV

Reference20 articles.

1. Müller D. Motion 20.3211: Für mehr Handlungsspielraum bei der Beschaffung von Medizinprodukten zur Versorgung der Schweizer Bevölkerung.

2. House of Commons. Financial Statement and Budget report, debated on Wednesday 15 March 2023; Available from: https://hansard.parliament.uk/Commons/2023-03-15/debates/5603C6A5-C487-4D37-8658-F6403BF9E5A5/FinancialStatementAndBudgetReport.

3. Regulating medicines in a globalized world: The need for increased reliance among regulators,2020

4. WHO. WHO expert committee on specifications for pharmaceutical preparations: fifty-fith report: Annex 10 - good reliance practices in the regulation of Annex 10 - good reliance practices in the regulation of medical products: high level principles and considerations; 2022.

5. European Union. Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC; 2017.

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