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List of acronyms – P Brunel (Module 4 Quality & Clinical Trial Conduct and Data Handling) GCP Good Clinical Practice GMP Good Manufacturing Practice GLP Good Laboratory Practice GPP Good Publication Practice CRO Contract Research Organization DMC Data Monitoring Committee DSMB Data safety Monitoring Board SOP Standard Operating Procedure IEC Institutional Ethics Committee ERB Ethics Review Board CRA Clinical Research Associate CI Clinical Investigator QA Quality Audit PD Protocol Deviation CRF Case Report Form CAPA Corrective Action Prevention Action CDP Clinical Development Plan CTT Clinical trial team LF Line Function RAP Review Analysis Plan MOP Manual of Operating Procedure RACI Responsible Accountable Consulted Informed RDP Resource Decision Point IPS Integrated Product Strategy QM Quality manual ICH International Conference on harmonization PAHO Pan American Health Organization WHO World Health Organization FDA Food and Drug Administration
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