Office For Medicinal Products Medical Devices And Biocides Poland

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The Office | Urząd Rejestracji Produktów Leczniczych, …

https://www.urpl.gov.pl/en/office

In accordance with the Act of 18 March 2011 on the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (Journal of Laws …

Urząd Rejestracji Produktów Leczniczych, Wyrobów …

https://urpl.gov.pl/en

Communication of the President of the Office of 20 October 2022 on the recommendation of the Committee for Medicinal Products for Human Use (CHMP) EMA on the use of …

National Helpdesks - ECHA - Europa

https://www.echa.europa.eu/-/poland-helpdesk

Poland. BPR helpdesk The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products al. Jerozolimskie 181c 02-222 Warsaw Telephone: +48 …

Registration under national procedure | Urząd Rejestracji …

https://urpl.gov.pl/en/biocidal-products/biocidal-products-registration/registration-under-national-procedure

I. Registration of biocidal products according to the national procedure is applicable for products containing at least one active substance, which is still under …

Medical Device Registration in Poland - omcmedical.com

https://omcmedical.com/medical-device-registration-in-poland/

Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (URPL) Medical Device Regulation: Act on Medical Devices (May 20, 2010) (Journal of …

Polish Regulation on Medical Devices: an …

https://www.regdesk.co/polish-regulation-on-medical-devices-an-overview/

The Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products (URPL), the Polish regulating authority in the sphere of medical …

Poland Medical Device Registration and Approval

https://arazygroup.com/medical-device-registration-poland/

The Polish Ministry of Health (MOH) must also be notified of all medical and IVD devices which are marketed in Poland. CLASSIFICATION SYSTEM: Medical …

Office for the Registration of Medicinal products, Medical Devices …

https://uk.practicallaw.thomsonreuters.com/5-503-6077?contextData=(sc.Default)

The Office is responsible for taking steps leading to decisions being adopted by the Minister of Health on the marketing of a medicinal product, giving information about the …

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