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  2. File:The Medical Devices Regulations 2002 (UKSI 2002-618).pdf

    en.wikipedia.org/wiki/File:The_Medical_Devices...

    English: These Regulations contain the legislative measures necessary for the implementation of three European Community Directives- Council Directive 90-385-EEC on the approximation of the laws of the Member States relating to active implantable medical devices, as amended; Council Directive 93-42-EEC concerning medical devices, as amended; and Directive 98-79-EC of the European Parliament ...

  3. Managed detection and response - Wikipedia

    en.wikipedia.org/wiki/Managed_detection_and_response

    Managed detection and response (or MDR) is a type of cybersecurity service providing customers with a cyberdefense technology and the associated remotely delivered human expertise. Those services help organizations monitor, detect, analyze and respond to advanced cyber threats. [1] [2] [3] MDR is a form of managed security service (MSS).

  4. List of PDF software - Wikipedia

    en.wikipedia.org/wiki/List_of_PDF_software

    A PDF creator and virtual PDF printer for Microsoft Windows PDF-XChange: Proprietary: Yes: PDF Tools allows creation of PDFs from many types of source input (images, scans, etc.). The PDF-XChange print driver allows printing directly to a PDF. A "lite" version of the print driver is free for non-commercial (home and academic) use. PrimoPDF ...

  5. PDF24 Creator - Wikipedia

    en.wikipedia.org/wiki/PDF24_Creator

    PDF24 Creator is an application software by Geek Software GmbH for the creation of PDF files from any application and for converting files to the PDF format. The application is released under a proprietary freeware license.

  6. Regulation (EU) 2017/745 - Wikipedia

    en.wikipedia.org/wiki/Regulation_(EU)_2017/745

    Regulation (EU) 2017/745 is a regulation of the European Union on the clinical investigation and placing on the market of medical devices for human use. It repealed Directive 93/42/EEC on Medical Devices (MDD) and Directive 90/385/EEC on active implantable medical devices (AIMDD).

  7. Medical device reporting - Wikipedia

    en.wikipedia.org/wiki/Medical_device_reporting

    Medical device reporting (MDR) is the procedure for the Food and Drug Administration to get significant medical device adverse events information from manufacturers, importers and user facilities, so these issues can be detected and corrected quickly, and the same lot of that product may be recalled.