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Laboratory Data System Training Courses In North America

1 training items found
21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials

21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials

by:ComplianceOnline   based inSan Jose, CALIFORNIA (USA)
Conducting clinical trials in a rapidly evolving electronic environment presents a unique challenge to the medical device industry where not only quality (GLP/GMP) plays an essential role – but collecting accurate, maintaining viable data (GCP) as part of continuous process improvement (while mitigating risk) is an essential and critical component of the development paradigm. The complexity ...
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