Pharmacovigilance & Drug Safety Vendors

“Establish a single global safety database with unified end-to-end workflows, secure cloud-based architecture, and open integrations.”

“PLG can run end-to-end pharmacovigilance, including case processing, signal management, periodic safety reports and local safety representation in the countries where your product…”

“At Althian, our pharmacovigilance team provides end-to-end drug safety support — during clinical trials and beyond, into the post-approval lifecycle. We combine deep regulatory…”

“Our pharmacovigilance business is one of the largest groups of PV experts worldwide, with a combination of deep life sciences expertise and best-in-class technologies. So you can…”

“We offer comprehensive clinical safety solutions including case processing from intake through regulatory submission, aggregate safety reports, contribution to clinical trial…”

“…Centralize literature reviews, smart filter by adverse event or geography, and manage workflows for triage and regulatory action—all in one clean dashboard.”

“Our flexible approach and commitment to timely case reporting allow clients to use our PV experts to handle all or parts of drug safety reporting responsibilities.”

“Within one system, sponsors and CROs process and manage global and domestic adverse events for drug, biologic, vaccine, device, and combination products.”

“Navigate the complexities of signal management with confidence and compliance. Manage, report, and share signal information with transparency and accuracy in EVIDEX® fully…”

“TikaMedInfo empowers Medical Affairs teams with AI-driven workflows to seamlessly manage requests, route adverse events, ensure compliance, and deliver the right information to…”

“Adverse Event Signal Detection: Federated AI analytics identify emerging safety trends weeks earlier, shifting PMS from reactive monitoring to predictive risk mitigation.”

“PV system & process architecture PV organizational design &/or sourcing strategy”

“Halloran conducts numerous Good Practice (GxP) audits of clinical trial vendors and suppliers, including Laboratories, CDMOs, CROs, clinical supply depots, and safety and…”

“Integrated summaries of safety/efficacy Annual and periodic safety reports”

“…Pediatric Investigation Plans (PIP)/Ped Plans (PSP) Post-authorisation Safety Study (PASS) Aggregated safety reporting Risk Management Plans (RMP)”

“IND annual reports (DSUR) and maintenance”

“…Using our innovative signal detection methodology, we can quickly identify safety signals relating to your product and evaluate the associated context.”

“Since 1999, we have been analyzing healthcare data to identify side effects earlier, improve patient safety and outcomes, and guide better treatment decisions.”