Comparator products in Bioequivalence/Therapeutic Equivalence studies

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Brexit, Health And Social Care

Published

December 31, 2020

Last updated

December 31, 2020

Description

This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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