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The conference provides a platform for panel discussions and the presentation of peer-reviewed information systems research papers. The first HICSS conference took place in 1968 at the University of Hawaii, with the goal to promote collaborative research on computer science, information technology, and telecommunications. Notably, the first six ...
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.
In the standard preregistration format, researchers prepare a research protocol document prior to conducting their research. Ideally, this document indicates the research hypotheses, sampling procedure, sample size, research design, testing conditions, stimuli, measures, data coding and aggregation method, criteria for data exclusions, and statistical analyses, including potential variations ...
The GHC conference has been criticized for a lack of diversity, particularly racial diversity, [21] and financial inaccessibility due to the high cost of attendance. [22] [23] In 2019, the cost of registration, not including hotel, transportation, or other costs, was $450 for students, $600 for academics, and $1,150 for general registration. [24]
March 14–18, 2022: HIMSS Global Health Conference and Exhibition, Orlando, Florida. [12] August 8–13, 2021: HIMSS Global Health Conference and Exhibition, Las Vegas, Nevada. [13] March 9–13, 2020: HIMSS Global Health Conference and Exhibition, Orlando, Florida. [14] The conference had been canceled due to the coronavirus outbreak. [15]
[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]
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]
In the 1980s, the European Union began harmonising regulatory requirements. In 1989, Europe, Japan, and the United States began creating plans for harmonisation. The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) was created in April 1990 at a meeting in Brussels.