Post-Authorization Safety & Effectiveness Studies Vendors
Compare partners for post-authorization safety and effectiveness studies (PASS and PAES) on real-world safety, effectiveness and use after approval.
Related workflows
CRO / Research Services Provider · +1 more type
Althian Clinical Research is a boutique CRO supporting clinical trials, regulatory submissions, safety, data, and real-world studies in Mexico and LATAM.
Evidence-backed capability match
“…Post-Marketing Surveillance Studies Following product approval, we conduct post-marketing surveillance studies to monitor safety and effectiveness in real-world conditions —…”Source: althian.com
Also offers: Full-Service Clinical Trial Execution (CRO Services), Marketing Authorization & Lifecycle Submission Support, +3 more
CRO / Research Services Provider · +7 more types
IQVIA is a CRO and technology provider delivering clinical trials, real-world evidence, commercial intelligence and safety operations.
Products: IQVIA Vigilance Platform, SmartSolve +4 more
Evidence-backed capability match
“Post Authorization Safety Studies are designed to identify or quantify safety risks, confirm safety profiles, or evaluate the effectiveness of risk management measures for…”Source: iqvia.com
Also offers: Full-Service Clinical Trial Execution (CRO Services), Real-World Data Platform, +6 more
Consulting / Advisory Firm · +4 more types
Lumanity is a life sciences consultancy for market access strategy, health economic modeling, brand positioning and scientific communications.
Products: Lumanity Illuminator, Evidence Illuminator +9 more
Evidence-backed capability match
“Post-authorization safety and efficacy studies (PASS/PAES) and drug utilization review (DUR)”Source: lumanity.com
Also offers: Market Access Strategy & Launch Planning, Brand Strategy & Positioning, +2 more
Compare listed vendors
What this covers: Post-authorization studies designed to evaluate real-world safety, effectiveness, utilization, or risk-management questions after product approval.
| Vendor | Delivery model | Also offers | In their words |
|---|---|---|---|
| Althian Clinical Research | CRO / Research Services Provider | RWE Study Operations & Vendor Management | “…Post-Marketing Surveillance Studies Following product approval, we conduct post-marketing surveillance studies to monitor safety and effectiveness in…”althian.com · reviewed Oct 24, 2026 |
| IQVIA | CRO / Research Services Provider | RWE Study Operations & Vendor Management | “Post Authorization Safety Studies are designed to identify or quantify safety risks, confirm safety profiles, or evaluate the effectiveness of risk management…”iqvia.com · reviewed Oct 19, 2026 |
| Lumanity | Consulting / Advisory Firm | RWE Study Operations & Vendor Management | “Post-authorization safety and efficacy studies (PASS/PAES) and drug utilization review (DUR)”lumanity.com · reviewed Oct 21, 2026 |