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