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  2. Accreditation Council for Continuing Medical Education

    en.wikipedia.org/wiki/Accreditation_Council_for...

    The ACCME's mission is to provide those in the medical field with opportunities to maintain competence and learn about new and developing areas of their field. A voluntary self-regulated system and a peer-review process are used to regulate and accredit medical education providers. The primary responsibilities of the ACCME are to: [3]

  3. CE marking - Wikipedia

    en.wikipedia.org/wiki/CE_marking

    CE marking example on a mobile phone charger. The presence of the logo (from French, "conformité européenne" meaning "European conformity") [2] on commercial products indicates that the manufacturer or importer affirms the goods' conformity with European health, safety, and environmental protection standards.

  4. Continuing medical education - Wikipedia

    en.wikipedia.org/wiki/Continuing_medical_education

    Continuing medical education (CME) is continuing education (CE) that helps those in the medical field maintain competence and learn about new and developing areas of their field. These activities may take place as live events, written publications, online programs, audio, video, or other electronic media.

  5. Commission on Accreditation of Healthcare Management ...

    en.wikipedia.org/wiki/Commission_on...

    Founded in 1968 as the Accrediting Commission on Education for Health Services Administration (ACEHSA), it adopted its current name in 2004 to reflect a change in strategic direction. This came after its 2001 Orlando Forum, a meeting funded by the Kellogg Foundation and the Robert Wood Johnson Foundation and called to examine management and ...

  6. Notified body - Wikipedia

    en.wikipedia.org/wiki/Notified_Body

    CE Mark. A notified body, in the European Union, is an organisation that has been designated by a member state to assess the conformity of certain products, before being placed on the EU market, with the applicable essential technical requirements. These essential requirements are publicised in European directives or regulations.

  7. Type approval - Wikipedia

    en.wikipedia.org/wiki/Type_approval

    Type approval or certificate of conformity is granted to a product that meets a minimum set of regulatory, technical and safety requirements. Generally, type approval is required before a product is allowed to be sold in a particular country, so the requirements for a given product will vary around the world.

  8. Certification mark - Wikipedia

    en.wikipedia.org/wiki/Certification_mark

    Canadian certification label on a bag of rockwool Counterfeit electrical cords with false UL certification marks. A certification mark on a commercial product or service is a registered mark that enables its owner ("certification body") to certify that the goods or services of a particular provider (who is not the owner of the certification mark) have particular properties, e.g., regional or ...

  9. Product certification - Wikipedia

    en.wikipedia.org/wiki/Product_certification

    product certifications (many nations) Product certification or product qualification is the process of certifying that a certain product has passed performance tests and quality assurance tests, and meets qualification criteria stipulated in contracts, regulations, or specifications (sometimes called "certification schemes" in the product certification industry).