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  2. Clinical officer - Wikipedia

    en.wikipedia.org/wiki/Clinical_officer

    The Clinical Officers (Training, Registration and Licensing) Act No.20 of 2017 is the law that governs the medical practice of a clinical Officer. [28] It establishes the Clinical Officers Council whose functions are to: advise the government on policy matters relating to clinical medicine practice

  3. Health professional requisites - Wikipedia

    en.wikipedia.org/wiki/Health_professional_requisites

    For instance, in the United States, under Michigan state laws, an individual is guilty of a felony if he practices or holds himself out as practicing a health profession subject to regulation without a license or registration or under a suspended, revoked, lapsed, void, or fraudulently obtained license or registration, or exceeding what a ...

  4. Clinical Officers Council - Wikipedia

    en.wikipedia.org/wiki/Clinical_Officers_Council

    The Clinical Officers Council of Kenya (COC) is a government agency – a corporate body created by the Clinical Officers (Training, Registration and Licensing) Act no. 20 of 2017 – Laws of Kenya whose work is to supervise and control the training and professional practice of medicine, dentistry, orthopaedics and health work by clinical officers and to register and license clinics and ...

  5. 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

  6. Trial master file - Wikipedia

    en.wikipedia.org/wiki/Trial_master_file

    The minimum essential documents that are required for the registration of pharmaceutical products designed for human use are specified in the document 'ICH Good Clinical Practices,' published in 1997 by the ICH [2] Example ICH essential documents that would be required in any US, EU or Japan based clinical trial would include: signed protocol ...

  7. Electronic common technical document - Wikipedia

    en.wikipedia.org/wiki/Electronic_Common...

    The electronic common technical document (eCTD) is an interface and international specification for the pharmaceutical industry to agency transfer of regulatory information. The specification is based on the Common Technical Document (CTD) format and was developed by the International Council for Harmonisation (ICH) Multidisciplinary Group 2 ...

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  9. Educational Commission for Foreign Medical Graduates

    en.wikipedia.org/wiki/Educational_Commission_for...

    According to the US Department of Education, the Educational Commission for Foreign Medical Graduates (ECFMG) is "the authorized credential evaluation and guidance agency for non-U.S. physicians and graduates of non-U.S. medical schools who seek to practice in the United States or apply for a U.S. medical residency program.