Prioritizing safety is fundamental throughout every phase of clinical trials

Ensuring ongoing safety monitoring is vital from the earliest stages of pharmaceutical development and throughout the product life cycle. Our long experience means we can offer fast and reliable development of safety management plans with smooth execution.

  • Full Service Support from Start to Finish
  • Preparation and Submission of Development Safety Update Report (DSUR)
  • Safety Management Plan (SMP) Development/ Maintenance
  • SUSAR/SAE Management, including Reporting to Competent Authorities and Ethics Committees
  • Expertise in Safety Database Management

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