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[1] [2] Based in Arlington, Virginia, United States, ECI is devoted to the advancement of high ethical standards and practices in public and private institutions, and provides research about ethical standards, workplace integrity, and compliance practices and processes. [3]
Created in 1999, the CIP program is a result of many years of discussions and planning by organizational members and leaders. It is endorsed by federal regulatory officials, professional associations, many national advisory bodies and IRB professionals who are committed to improving the quality of human research protection programs.
At an organizational level, it is achieved through management processes which identify the applicable requirements (defined for example in laws, regulations, contracts, strategies and policies), assess the state of compliance, assess the risks and potential costs of non-compliance against the projected expenses to achieve compliance, and hence ...
The Health Care Consent Act (HCCA) is an Ontario law concerned with the capacity to consent to treatment and admission to care facilities. (i.e., informed consent ). [ 1 ] [ 2 ] As of 2 August 2023 [update] on a date to be named by proclamation of the Lieutenant Governor, the act will also apply to confining in a care facility.
Legal compliance is the process or procedure to ensure that an organization follows relevant laws, regulations and business rules. [5] The definition of legal compliance, especially in the context of corporate legal departments, has recently been expanded to include understanding and adhering to ethical codes within entire professions, as well.
The eighth revision of Helsinki (2024) newly highlights the roles of global inequities in medical research and includes a new statement that scientific integrity "is essential in the conduct of medical research involving human participants. Involved individuals, teams, and organizations must never engage in research misconduct". [7]
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]
The IMS/ASA Spring Research Conference (SRC) is an annual conference sponsored by the American Statistical Association (ASA) Section on Physical and Engineering Sciences (SPES) [1] and the Institute of Mathematical Statistics (IMS). [2] The goal of the SRC is to promote cross-disciplinary statistical research in engineering, science and technology.