Drug database
Manuals RZPRO
- 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