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006 m o d
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008 241013s2025 xx o 0|| 0 eng d
040 _aOCoLC-P
_beng
_cOCoLC-P
020 _a9781040166277
_q(electronic bk.)
020 _a104016627X
_q(electronic bk.)
020 _a9781003407010
_q(electronic bk.)
020 _a1003407013
_q(electronic bk.)
020 _a9781040166260
_q(electronic bk. : PDF)
020 _a1040166261
_q(electronic bk. : PDF)
020 _z1032524073
020 _z9781032524078
024 7 _a10.1201/9781003407010
_2doi
035 _a(OCoLC)1460454995
035 _a(OCoLC-P)1460454995
050 4 _aR853.C55
072 7 _aMED
_x071000
_2bisacsh
072 7 _aMED
_x072000
_2bisacsh
072 7 _aTDCW
_2bicssc
245 0 0 _aGOOD CLINICAL PRACTICES IN PHARMACEUTICALS
_h[electronic resource].
260 _a[S.l.] :
_bCRC PRESS,
_c2025.
300 _a1 online resource
490 1 _aDrugs and the pharmaceutical sciences
520 _aGood 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.
588 _aOCLC-licensed vendor bibliographic record.
650 0 _aClinical trials.
_963521
650 7 _aMEDICAL / Pharmacology
_2bisacsh
_964250
650 7 _aMEDICAL / Pharmacy
_2bisacsh
700 1 _aBunn, Graham P.,
_eeditor.
_994304
830 0 _aDrugs and the pharmaceutical sciences.
_964867
856 4 0 _3Taylor & Francis
_uhttps://www.taylorfrancis.com/books/9781003407010
856 4 2 _3OCLC metadata license agreement
_uhttp://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf
942 _cE-Books
999 _c67767
_d67767