Why Drug Accountability Matters in Clinical Trials

Drug accountability is a critical aspect monitored by the FDA at clinical trial sites. Principal investigators must maintain and document control over investigational products, ensuring they are only administered under direct supervision. Clinical research organizations also conduct routine audits to verify drug accountability. However, instances of improper disposal or false certifications have been identified, highlighting the importance of vigilance in maintaining accurate drug records. Compliance with drug accountability regulations is essential, as both the FDA and the Department of Justice oversee this area closely. For assistance with clinical trial compliance, reach out to us!Support the show

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