Pharmacovigilance for Clinical Trials
Purpose-built for pharmaceutical companies
Enhancing Clinical Trials with Social Listening
Social listening plays a vital role in pharmacovigilance during clinical trials by uncovering patient experiences, feedback, and safety concerns as they happen. This real-time visibility enables faster detection of issues and supports trial integrity.
Early Detection of Adverse Events
Monitor participant feedback for signs of tolerability issues or unexpected side effects.
Improved Trial Safety Oversight
Quickly escalate safety concerns to investigators and sponsors.
Better Participant Engagement
Address patient concerns and improve retention through active listening and communication.
Define Monitoring Objectives
Identify what patient conversations and data points are relevant to your trial phase.
Monitor Patient Channels
Track discussions in forums, social media, and health communities where trial participants may share feedback.
Route Insights into Trial Protocols
Feed detected signals into safety review processes and adapt protocols as needed.
More Agile Trial Management
Identify safety trends early and adapt quickly to protect participants.
Improved Regulatory Alignment
Maintain accurate, timely safety reporting across global trial sites.
Higher Participant Trust
Build credibility by showing responsiveness to patient concerns during the trial lifecycle.