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Monitoring and Ensuring Compliance in the Life Sciences (PH113)
Pharma compliance, compliance teams, regulations, regulatory authorities, Office of Inspector General, OIG, OIG guidelines, standards, guidances, firewalls, public scrutiny, pharma industry reputation, risk assessment, monitoring, internal audits, pharmaceutical restructuring, compliance training, compliance testing, corporate integrity agreement, standard operating procedures, SOPs, oversight, live monitoring, SOP, centralization, business ethics, ethical practices, key opinion leaders, thought leaders, medical science liaisons, documentation, transparency, medical groups, medical affairs, quality assurance, PhRMA Code, Uniform Requirements, International Committee of Medical Journal Editors, ICJME, Good Publication Practices, GPP, Consort Statement, FDA, Food and Drug Administration Act, FDAMA, Good Clinical Practices, GCP, compliance best practices
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