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CTSA Institution

University of California, Davis

Disclaimer Please cite the appropriate authors/contacts when using or adapting these materials.
Acknowledgment Daniel Redline, BA, CCRP, CCRC
Associate Manager
Clinical Affairs
Dey, LP
UC Davis RCR Responsible Conduct of Research Lecture Series
Contacts Debie Schilling, Analyst, Clinical Trials, Clinical & Translational Science Center (CTSC)
Format PDF
URL Download
Materials Provided PDF (27 PowerPoint? Slides)
Title The Essentials of Good Clinical Practice (GCP)
Topics Description This presentation covers the guidelines referred to as GCPs , which prevent harm to study participants by setting forth established guidelines for the investigator and the research staff on how to perform valid, productive, ethical biomedical research with integrity.
Keywords Analyzing; Auditing; Clinical Trials; Conducting; Confidentiality of Subjects; Designing; Federal Regulations; Good Manufacturing Practice (GMP); Informed Consent; Institutional Review Board (IRB); International Conference on Harmonization (ICH); Investigator; Investigator’s Brochure; Monitoring; Performing; Protect Public Health; Protocol; Recording; Reporting; Sponsor; Standard Operating Procedures (SOPs); State and Local Laws
See Also

Topic Data Acquisition Management Sharing and Ownership, Human Subjects, Collaborative Science, Other
Topic revision: r4 - 28 Jul 2009 - 11:31:13 - NancyHills
ResearchEthics.The_Essentials_Of_Good_Clinical_Practice moved from ResearchEthics.TheEssentialsOfGoodClinicalPractice on 06 Jul 2009 - 19:01 by CTSpediaAdmin - put it back
 
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