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  1. 25 lis 2024 · Chronimy zdrowie i dbamy o bezpieczeństwo społeczeństwa w obszarach produktów leczniczych, wyrobów medycznych i produktów biobójczych. Poprzez URPL możesz zarejestrować produkt leczniczy, zgłosić lek do kontroli oraz zgłosić działanie niepożądane leku.

  2. Releasable establishment registration and listing information under the Freedom of Information Act is available by searching the Establishment Registration and Listing database. The database...

  3. If you have applied for a European Health Insurance Card (EHIC) via an Internet Patient Account (IKP) or via the Electronic Platform for Public Administration Services (ePUAP), you can keep track of the status of your application.

  4. 14 mar 2023 · Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices introduce an EU device identification

  5. The ICTRP Search Portal aims to provide a single point of access to information about ongoing and completed clinical trials. It provides a searchable database containing the trial registration data sets made available by data providers around the world meeting criteria for content and quality control.

  6. There are two types of clinical studies: interventional studies (also called clinical trials) and observational studies. The unique identification code given to each clinical study upon registration at ClinicalTrials.gov. The format is "NCT" followed by an 8-digit number (for example, NCT00000419).

  7. 9 gru 2023 · Access the "Provider Enrollment" section of the Noridian Medicare Portal (NMP) to view application status explanations, upload additional requested information, and download a completed notification letter.

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