Swissmedic
The new article outlines the reporting requirements to be followed by the parties responsible for clinical investigations conducted in Switzerland.
Medsafe
The article highlights the key points related to the regulatory requirements for clinical trials in New Zealand.
BfArM
The article provides an overview of the authorization process for clinical trials involving medical devices to be conducted in Germany.
HSA
The article provides a brief overview of the regulatory requirements in the sphere of clinical evaluation of healthcare products.
FDA
The article highlights the aspects related to the rights and responsibilities of Institutional Review Boards in the context of informed consent. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere...
Gartner® Market Guide for Life Science Regulatory Information Management Solutions
Download NowGartner® Market Guide for Regulatory Intelligence Solutions
Download Now
