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Volumn 81, Issue 2, 2006, Pages 146-153

A program to provide regulatory support for investigator-initiated clinical research

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL RESEARCH; FOOD AND DRUG ADMINISTRATION; HEALTH CENTER; HEALTH PROGRAM; MEDICAL LITERATURE; PRIORITY JOURNAL; REVIEW; UNITED STATES; ARTICLE; CLINICAL TRIAL; DOCUMENTATION; DRUG APPROVAL; DRUG SCREENING; GOVERNMENT REGULATION; HUMAN; LEGAL ASPECT; MEDICAL RECORD; METHODOLOGY; ORGANIZATION AND MANAGEMENT; PERSONNEL; PROGRAM DEVELOPMENT; SAFETY; UNIVERSITY HOSPITAL;

EID: 33645836520     PISSN: 10402446     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001888-200602000-00009     Document Type: Review
Times cited : (8)

References (23)
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    • 21 C.F.R. § 812.2(m) (2005).
  • 5
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    • 21 C.F.R. § 312.2(b)(1) (2005).
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    • 21 C.F.R. § 812.2(b) (2005).
  • 8
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    • 21 C.F.R. § § 312.23, 812.20 (2005)
    • 21 C.F.R. § § 312.23, 812.20 (2005).
  • 10
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    • (1998) Guidance on IDE Policies and Procedures
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    • Holobaugh, Patricia, chief, bioresearch monitoring branch, FDA/CBER/Office of Compliance and Biologics Quality. Personal communication, August 23, 2005
    • Holobaugh, Patricia, chief, bioresearch monitoring branch, FDA/CBER/Office of Compliance and Biologics Quality. Personal communication, August 23, 2005.
  • 13
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    • 21 C.F.R. § 312.2(b)(1)(iii) (2005).
  • 14
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    • 21 C.F.R. § 812.3(m) (2005).
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    • 21 C.F.R. § § 312.2, 812.2 (2005).
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    • Johns Hopkins admits Fault in Fatal Experiment
    • July 17
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.