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Quality Assurance Systems, Inc.
clinical quality assurance,
CQA, quality assurance, QA, good clinical practices, GCP, Food & Drug Administration,
Food and Drug Administration, FDA, clinical trials, audit, auditing, audits,
good laboratory practices, GLP, investigator site audits, trial center, trial site,
contract research organization, CRO, sponsor company, pharmaceutical company,
standard operating procedures, SOP, SOPs, CFR Part 11 audits, CFR Part 11 training,
GCP training, GLP training, auditing training, inspection readiness assessment,
regulatory inspections, NDA, BLA, PMA, data management audits, database audits,
biostatistics audits, programming audits, for-cause audits, for cause audits,
directed audits, core laboratory audits, core lab audits, biotech companies,
medical device companies, studies, trials, Phase I clinical trials,
Phase II clinical trials, Phase III clinical trials, Phase IV clinical trials,
Phase I clinical studies, Phase II clinical studies, Phase III clinical studies,
Phase IV clinical studies, trial master files, trial master central files,
trial master essential documents, institutional review board audits
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