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.