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2. Template:European Standards - Wikipedia

   en.wikipedia.org/wiki/Template:European_Standards

   Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

3. Consolidated Clinical Document Architecture - Wikipedia

   en.wikipedia.org/wiki/Consolidated_Clinical...

   Consultation Note - The Consultation Note is generated by a request from a clinician for an opinion or advice from another clinician. [ 7 ] Continuity of Care Document - The Continuity of Care Document (CCD) represents a core data set of the most relevant administrative, demographic, and clinical information facts about a patient's healthcare ...

4. Standing Committee of European Doctors - Wikipedia

   en.wikipedia.org/wiki/Standing_Committee_of...

   The Standing Committee of European Doctors (French: Comité Permanent des Médecins Européens, CPME) represents national medical associations across Europe. It promotes the highest standards of medical training and medical practice in order to achieve the highest quality of health care for all patients in Europe.

5. List of style guides - Wikipedia

   en.wikipedia.org/wiki/List_of_style_guides

   Council of Europe - English Style Guide, by the Council of Europe [2] English Style Guide ("A handbook for authors and translators in the European Commission" – executive branch of the European Union.) [3] Interinstitutional Style Guide. [4]

6. Good documentation practice - Wikipedia

   en.wikipedia.org/wiki/Good_documentation_practice

   Scrap paper, Post-it notes – intentionally recording raw data on non-official records is a set-up for transcription and is therefore prohibited. Avoiding asterisks as part of the notation of a hand-change – where insufficient white space permits a fully notated hand change, a common practice is to use an asterisk (or other mark) near the ...

7. Common Technical Document - Wikipedia

   en.wikipedia.org/wiki/Common_Technical_Document

   The Common Technical Document (CTD) is a set of specifications for an application dossier for the registration of medicine, designed for use across Europe, Japan, the United States, and beyond. [ 1 ] Major Synopsis

8. Medical Devices Directive - Wikipedia

   en.wikipedia.org/wiki/Medical_Devices_Directive

   The Medical Device Directive—Council Directive 93/42/EEC of 14 June 1993 concerning medical devices—is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently in order for a manufacturer to legally place a medical device on the European market the ...

9. Template:European Article Number/doc - Wikipedia

   en.wikipedia.org/wiki/Template:European_Article...

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