Services
Pharmacovigilance & Safety Monitoring
Patient safety handled with rigour: adverse event collection, assessment and reporting within regulatory timelines, throughout your study.
Request a proposal →Safety reporting in Indian trials runs to strict timelines involving the sponsor, ethics committee and regulator. ACRS manages that flow so nothing is missed.
Clinical trial safety
- Medical and safety monitoring
- AE and SAE collection and follow-up
- Expedited SAE reporting to sponsors, ethics committees and regulators
- Safety data reconciliation with the clinical database
Discuss pharmacovigilance for your study
Tell us about your protocol, timelines and therapeutic area, and we will suggest how ACRS can support it.