Request

“1. Details of the informed consent process employed in Scotland for medicinal products within Conditional Authorisation and/or Emergency Use Authorisation.”

“2. Details of any directives to alter that process for any specific drugs under Conditional Authorisation and/or Emergency Use Authorisation, including the names of those CA/EUA drugs, dates and correspondence showing the directives given with regards to obtaining informed consent for these products.”

Last updated: 06 December 2024