Home / Dz.U. 2016 poz. 209
Regulation of the Minister of Health of February 16, 2016, on the detailed requirements for planning, conducting, monitoring, and documenting clinical investigations of medical devices
Rozporządzenie Ministra Zdrowia z dnia 16 lutego 2016 r. w sprawie szczegółowych wymagań dotyczących planowania, prowadzenia, monitorowania i dokumentowania badania klinicznego wyrobu medycznego
Type
Regulation (Rozporządzenie)
Status
in force (obowiązujący)
Announced
2016-02-16
Entry into force
2016-02-20
Texts
The consolidated text (tekst ujednolicony) is unofficial; only the signed PDFs from Dziennik Ustaw / Monitor Polski are legally authentic.
Keywords
Medical Productsmonitoringmedical documentation
Related acts
Legal Basis (1)
Legal Basis from Art. (1)
- Law of May 20, 2010 on medical devices · art. 41 ust. 4
Repeals Resulting From (1)
- Law of April 7, 2022, on medical devices · 2030-05-26
Acts referring to this act
- Acts Declared Repealed: Law of April 7, 2022, on medical devices
- Implementing Regulations: Law of May 20, 2010 on medical devices