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The Office | Urząd Rejestracji Produktów …

    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 2011, No 82, item 451, as amended), the statutory activities of the Office include three core areas: – carrying out procedures and activities involving medicinal products for human use and veterinary medicinal products, in particular:

Information about the Office | Urząd Rejestracji …

    https://urpl.gov.pl/en/office/information-about-office
    The President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products is a central government administrative authority …

Importing Medical Devices | FDA

    https://www.fda.gov/industry/importing-fda-regulated-products/importing-medical-devices
    Registration and listing. Establishments that are involved in the production and distribution of …

Contact - Urząd Rejestracji Produktów Leczniczych, …

    https://www.urpl.gov.pl/en/office/contact
    The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products Al. Jerozolimskie 181C 02-222 Warszawa phone number + 48 22 492 …

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 …

Medical Devices | FDA - U.S. Food and Drug Administration

    https://www.fda.gov/Medical-Devices
    Approvals and clearances, information on medical devices by type Digital Health Center of Excellence Cybersecurity, mobile medical apps, wireless medical devices, AI/ML in …

The Office for Registration of Medicinal Products, …

    https://rocketreach.co/the-office-for-registration-of-medicinal-products-medical-devices-and-biocidal--department_b5de064cf42e4d56
    The The Office for Registration of Medicinal Products, Medical Devices and Biocidal management team includes Grzegorz Cessak (Member of Management Board), …

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 …

ODI Pharma receives approval from the Office for …

    https://news.cision.com/odi-pharma/r/odi-pharma-receives-approval-from-the-office-for-registration-of-medicinal-products--medical-devices,c3702397
    ODI Pharma receives approval from the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products in Poland to distribute and sell its …

Product registration - Competent Authority⚕️ MDR …

    https://mdrregulator.com/ce-marking/product-registration
    The manufacturer and an authorised representative residing or based in Poland is obliged to submit a medical device and a medical device for in vitro diagnostics. The notification …



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