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.