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In 2019, IFPMA released a strengthened code of ethics [5] and professional standards. [6] Among the revisions to the code is a prohibition on gifts provided to healthcare professionals. [ 7 ] The code revision has been followed by Ethoscope [ 8 ] – an open-source, continuously evolving resource that contains diverse guidance designed to keep ...
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 ...
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]
A code of practice is adopted by a profession (or by a governmental or non-governmental organization) to regulate that profession. A code of practice may be styled as a code of professional responsibility, which will discuss difficult issues and difficult decisions that will often need to be made, and then provide a clear account of what behavior is considered "ethical" or "correct" or "right ...
The meeting files, correspondences, and unpublished papers from the commission are currently held in the Bioethics Research Library Kennedy Institute of Ethics at Georgetown University. [2] Multiple government formed organizations continued to fulfill the commission's purposes after its expiration, most specifically the Bioethical Medical ...
The ethics involved within pharmaceutical sales is built from the organizational ethics, which is a matter of system compliance, accountability and culture (Grace & Cohen, 2005). Organizational ethics are used when developing the marketing and sales strategy to both the public and the healthcare profession of the strategy. [ 1 ]
Supporting documents can be added to the original document as an attachment for clarification or recording data. Attachments should be referenced at least once within the original document. Ideally, each page of the attachment is clearly identified (i.e. labeled as "Attachment X", "Page X of X", signed and dated by person who attached it, etc.)
The CMA Code of Ethics and Professionalism (Code) is a document produced by the Canadian Medical Association. The Code articulates the ethical and professional commitments and responsibilities of the medical profession in Canada. [1]