MHRA on Quarterly Summary Reporting
The article provides an overview of the current reporting requirements for healthcare products allowed to be used for clinical trials.
The article provides an overview of the current reporting requirements for healthcare products allowed to be used for clinical trials.
The article highlights the key points related to the regulatory requirements for combination studies intended to be carried out in Switzerland.
The new article provides further clarifications regarding the authorisation procedure to be followed by the parties interested in conducting combination studies in Switzerland.
The new article clarifies the approach to be followed when introducing modifications to combination studies already approved by Swissmedic.
The new article outlines the reporting requirements to be followed by the parties responsible for clinical investigations conducted in Switzerland.