The Safety Monitoring You Need to Minimize Trial Risk
Our team collaborates to minimize risks with effective monitoring, assessment and reporting of safety information throughout the duration of your clinical program.
Our pharmacovigilance services include:
Case processing for clinical trials, post-marketing, literature
Development of Risk Management Plans and Risk Evaluation and Mitigation Strategies (REMS)
Safety reviews of Clinical Protocols
Periodic report preparation
Manage and process adverse events documentation