Pharmacovigilance, risk management and training: our experts can guide you

Whether you need to collect and analyze the data from the monitoring of clinical trials or post-market surveillance, or offering training to your employees, SPharm has the resources you need. 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

You too can benefit from SPharm’s expertise!

You have questions concerning pharmacovigilance? Use the form below to contact us and we will respond promptly.

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