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Published By: Tripwire     Published Date: Jun 30, 2009
Find out how a robust configuration audit and control system can enable electronic submissions and signatures, and validate electronic data, in compliance with the FDA's mandatory submission of clinical trials records.
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tripwire, integrity, data, clinical, electronic, software, cfr11, trustworthiness, fda, solutions, solution, electronic systems, hipaa, policy, requirements
    
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