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yyissa@pharmaligent.com

Clinical Operations

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  • Protocols / Amendments / IB
  • TMF Documentation, Clinical Trial Monitoring
  • Transfer of Obligations (TOROs)
  • Protocol Deviations
  • Unexpected Events
  • Risk Management
  • CAPA design and processes
  • Project Management of audits including end-to-end strategy, document review and system integration.
  • Data and Report Audits
pharmaceutical risk assessment