Ethics in human researchToday, the principles of good clinical practice (GCP) form such an integral part of the development of new medicines that they could easily be taken for granted. Yet, the road to a universal code of ethics in human experimentation is paved with tragedies which have ...
The Association of the British Pharmaceutical Industry (ABPI) originally published its guidelines on Good Clinical (Research) Practice (GCP) in 1988. It has subsequently considered at length whether a revision of these guidelines was needed in view of the existence of GCP guidelines endorsed by ...
With the growing quest for answers to vexing dilemmas in critically ill patients, more intensive care units are embarking on clinical research. This places increasing importance on Good Clinical Research Practice (GCRP), a set of guidelines drawn up by the Pharmaceutical Industry to assist investigato...
The set of guidelines for good clinical research practice (GCRP) in pharmacodynamic studies of neuromuscular blocking agents, which was developed following an international consensus conference in Copenhagen, has been revised and updated following the second consensus conference in Stockholm in 2005. It ...
{Quality in Nuclear Medicine}, editor = {Glaudemans, Andor}, isbn = {978-3-319-33529-2}, language = {eng}, pages = {23--59}, publisher = {Springer International Publishing AG}, title = {Good Clinical Practices in (Nuclear) Research}, url = {http://dx.doi.org/10.1007/978-3-...
GCP, and provides guidance and assistance in the application and implementation of these principles by all parties involved in the clinical research process... A Barton - 《Journal of Epidemiology & Community Health》 被引量: 75发表: 2007年 Good clinical laboratory practice (GCLP): the need for...
Compliance with Good Clinical Practice (GCP) provides assurance that the rights, safety and well-being of trial subjects are protected, and that the results of the clinical trials are credible.
Clinical research is one of the important missions of an academic Albert Einstein medical centre and forms the cornerstone for improvement of healthcare. Funding for clinical research has increased steadily over the past few decades, both from the US government and the pharmaceutical industry. In thi...
consideredagood clinical practicebyregulatory authorities overseeing clinical research, [...] mdsol.com mdsol.com 临床监查员在试验机构核查原始文档向来被监管部门视为良好的临床实践操作,并且对于临床试验中保证数据质量而言也是极其重要。 mdsol.com mdsol.com ...
recording and reporting while continuing to ensure human subject protection and reliability of trial results. But, the changes have resounding effects on the conduct of clinical research by sponsors/CROs and investigators. As such, systematic analysis to ensure adherence to these clinical trial standards...