Manuály

User account creation

Manual No. 1 – First time login to the registry of medical devices and notification of a person

Manual No. 4 – Clinical investigations

How to register a Sponsor in the Registry of Medical Devices (RZPRO) and submit application for clinical investigation (CI) conduct when represented by a contract research organisation (CRO)

Application for Medical Device notification

Application for Medical Device change

Notification Activity extension

Application for medical device extension

Medical device notification according to Section 33 par. 2 of the Act on MD

Agency – request for access and power of attorney allocation

Application for clinical investigation change

Performance study module