The Swedish Medical Products Agency has certified the registration of the MedSciNet Clinical Trial Framework (CTF) as a Class I medical device meeting high safety and performance requirements.
Such registration is required for products with CE marking to declare their conformity with the standards for sale and use throughout the 30-country European Economic Area (EEA).
As stipulated by the Medical Products Agency, CE marking is a declaration that the product “achieves the performance intended by the manufacturer and meets high standards for the protection of life, personal safety, and health of patients and others”.
The MedSciNet CTF is a platform which enables organisations to host, develop, support, and manage multiple applications for clinical trials with minimal external support.
To learn more about CTF and other MedSciNet products, please visit our products page at medscinet.com/products.aspx