Access to Electronic Health Records by Sponsor representatives in clinical trials
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Health And Social Care
Published
November 26, 2020
Last updated
September 8, 2021
Description
The following guidance has been jointly developed by the Heath Research Authority (HRA) and MHRA, in consultation with the Information Commissioners Office (ICO), on behalf of the UK.
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 2.0 (United Kingdom)