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[9] [10] The former, published in 2016, sets the standards and guidance for the knowledge and skills required for non-medical healthcare professionals to deliver patient care. [11] [12] The latter, published in 2017, aimed to share best practice to facilitate local service redesign. [13]
The General Medical Council (GMC) is a public body that maintains the official register of medical practitioners within the United Kingdom.Its chief responsibility is to "protect, promote and maintain the health and safety of the public" by controlling entry to the register, and suspending or removing members when necessary.
Before any sanction is considered the GMC or MPTS must first be satisfied that a doctor's fitness to practise is currently impaired. If there is no impairment then a tribunal cannot impose a sanction, though they can and should consider whether a Warning should be issued where a doctor significantly departs from Good Medical Practice. [45]
In medical law and medical licensing, fitness to practise is a concept in the regulation of medicine regarding whether a health professional or social worker should be allowed to work. While fitness to practice can include matters of technical competence, including qualifications the concept also contains questions about the implications of the ...
The training standards for Foundation year 1 are published by the General Medical Council (GMC) :Outcomes for Provisionally Registered Doctors" (GMC July 2015). The two-year programmes are delivered within the national operational framework agreed by the Departments of Health. The curriculum is approved by the GMC. [13]
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It is conducted by the General Medical Council of the United Kingdom. The test is designed to assess the depth of knowledge and level of medical and communication skills possessed by the international medical graduates. The PLAB blueprint sets out what candidates are expected to demonstrate in the test and beyond. The PLAB test has 2 parts:
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]