The CCRP program was created to acknowledge a CRP's knowledge, understanding, and
application related to the conduct of clinical investigations involving humans in
accordance with the __________.
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International Council for Harmonisation (ICH) Guideline for Good Clinical
Practice, ICH Clinical Safety Data Management, the United States Code of
Federal Regulations (CFR) and the ethical principles that guide clinical
, research consistent with the principles of the Nuremberg Code, The Belmont
Report and the Declaration of Helsinki
Notice of inspection
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FDA Form 482
When was the CCRA (Clinical Research Associate) examination successfully
implemented?
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August 1995
Statement of the Investigator
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FDA Form 1572
Subject Matter Expert
application related to the conduct of clinical investigations involving humans in
accordance with the __________.
Give this one a try later!
International Council for Harmonisation (ICH) Guideline for Good Clinical
Practice, ICH Clinical Safety Data Management, the United States Code of
Federal Regulations (CFR) and the ethical principles that guide clinical
, research consistent with the principles of the Nuremberg Code, The Belmont
Report and the Declaration of Helsinki
Notice of inspection
Give this one a try later!
FDA Form 482
When was the CCRA (Clinical Research Associate) examination successfully
implemented?
Give this one a try later!
August 1995
Statement of the Investigator
Give this one a try later!
FDA Form 1572
Subject Matter Expert
