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Pharmacovigilance services

Whether you need to collect, analyze or report safety data from the monitoring of clinical trials or post-market surveillance, SPharm has the resources you need, including training for your employees. We will develop a customized work plan for your company’s specific needs – in order to provide you with the best possible support.

  • Clinical trials and post-marketing surveillance programs
  • Risk Management Plan (RMP)
  • Adverse drug reactions reporting and reconciliation, during clinical trials or after marketing
  • Canada Vigilance watch
  • Submission of: Periodic Safety Update
  • Reports (PSUR), Periodic Benefit Risk Evaluation Reports (PBRER)
  • Pharmacovigilance training

Find out what SPharm can do for you.

Learn how our proven expertise can help reach your objectives faster. Contact us today.