02703cam a2200493M 4500 9781003407010 FlBoTFG 20251030122244.0 m o d cr |n||||||||| 241013s2025 xx o 0|| 0 eng d OCoLC-P eng OCoLC-P 9781040166277 (electronic bk.) 104016627X (electronic bk.) 9781003407010 (electronic bk.) 1003407013 (electronic bk.) 9781040166260 (electronic bk. : PDF) 1040166261 (electronic bk. : PDF) 1032524073 9781032524078 10.1201/9781003407010 doi (OCoLC)1460454995 (OCoLC-P)1460454995 R853.C55 MED 071000 bisacsh MED 072000 bisacsh TDCW bicssc GOOD CLINICAL PRACTICES IN PHARMACEUTICALS [electronic resource]. [S.l.] : CRC PRESS, 2025. 1 online resource Drugs and the pharmaceutical sciences Good clinical practice (GCP) is a set of internationally recognized ethical and scientific quality requirements that must be followed when designing, conducting, recording, and reporting trials that involve the participation of human subjects. Compliance with GCP assures patients and the public that the rights, safety, and wellbeing of people taking part in studies are protected and that research data is reliable. Presents details on GCP, the international ethical, scientific, and practical standard to which all clinical research is conducted. Provides the most uptodate and best practices, techniques, and methodologies in good clinical practice. Discusses applicable laws and regulations supporting GCP compliance, quality and operations. Describes who is responsible for implementing and maintaining quality assurance and quality control systems to ensure that studies are conducted and data are generated, documented, and reported in compliance with the protocol. OCLC-licensed vendor bibliographic record. Clinical trials. 63521 MEDICAL / Pharmacology bisacsh 64250 MEDICAL / Pharmacy bisacsh Bunn, Graham P., editor. 94304 Drugs and the pharmaceutical sciences. 64867 Taylor & Francis https://www.taylorfrancis.com/books/9781003407010 OCLC metadata license agreement http://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf E-Books 67767 67767