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European Union: In the EU, Good Clinical Practice is backed and regulated by formal legislation contained in the Clinical Trial Regulation (Officially Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC). [3]
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. It provides ...
Kuala Lumpur Hospital. Healthcare in Malaysia is under the purview of the Ministry of Health of the Government of Malaysia. Malaysia generally has an efficient and widespread system of health care, operating a two-tier health care system consisting of both a government-run public universal healthcare system along with private healthcare providers.
Based on the accreditation of the Council on Education for Public Health (CEPH), an MPH or MSPH is not a clinical degree. [8] However, some states in the United States recognize MPH holders as ancillary clinical professionals (and patient-facing clinical staff) especially with regard to preventive medicine, health education, and other functions ...
The Ministry of Health (Malay: Kementerian Kesihatan; abbreviated MOH; Jawi: كمنترين كصيحتن ) is a ministry of the Government of Malaysia that is responsible for health system: health behaviour, cancer, public health, health management, medical research, health systems research, respiratory medicine, health promotion, healthcare tourism, medical device, [4] blood collection ...
The Malaysia Healthcare Travel Council (MHTC) was established by the Malaysian Ministry of Health in 2005. MHTC is responsible in advocating for the medical tourism industry in Malaysia. [ 1 ] In 2011, MHTC was incorporated as an independent entity to coordinate Malaysia's healthcare travel sector.
The Good Clinical Practice Directive (Directive 2005/28/EC of 8 April 2005 of the European Parliament and of the Council) lays down principles and detailed guidelines for good clinical practice as regards conducting clinical trials of medicinal products for human use, as well as the requirements for authorisation of the manufacturing or importation of such products.
WHO Good Clinical Laboratory Practice (GCLP) ISBN 978-92-4-159785-2; Stevens W. (2003) Good Clinical Laboratory Practice (GCLP): The need for a hybrid of Good Laboratory Practice and Good Clinical Practice guidelines/standards for medical testing laboratories conducting clinical trials in developing countries. Quality Assurance, 10: 83–89.