Your Trial Is Complex.Your Quality Strategy Shouldn't Be.
ABOUT VEDX CLINICAL
Built on Experience.Focused on Quality.
VedX Clinical brings together sponsor, CRO, investigator-site and Vendor experience to identify risk, strengthen quality and prepare clinical programs for regulatory scrutiny.
Based in China, with a global focus across APAC, Europe and the USA, we bring practical experience across global regulatory frameworks and health authorities, including FDA, EMA, MHRA and NMPA, with a strong focus on audit and inspection readiness.
- 01End-to-End Clinical Quality Expertise
- 02Practical, Risk-Based Approach
- 03Oncology & Complex Trial Experience
- 04Inspection-Ready, Patient-Focused Quality
WHERE WE GO DEEP
Complex Trials Demand Deeper Expertise.
Our deepest experience is in oncology and hematology, where complex protocols, novel mechanisms, adaptive designs and high-risk patient populations demand more from clinical quality.
VedX brings experience across immunology, rare disease and other complex therapeutic areas, giving sponsors access to specialists who understand both the clinical complexity and the quality systems behind it.
- Oncology & Hematology
- Immunology
- Rare Diseases
- Complex Clinical Programs
WHERE WE LIVE
Inspection Readiness Is Where We Live
We've prepared teams for FDA, EMA and NMPA inspections, supported front and back rooms, managed real-time requests, reviewed submissions and trained teams to answer difficult questions under pressure.
We know what inspectors look for because we've been in the room when they asked.
- Mock Inspections
- Front & Back Room Support
- Mock Interviews
- Storyboards
- Submission Review
- Inspection Training
- 20+ — Years of Combined Clinical & Quality Experience
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- 100+ — GCP/GxP, Vendor, Site & System Audits
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- 30+ — Countries in Our Global Consultant Network
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- 20+ — Regulatory & Inspection Experiences. FDA • EMA • NMPA & Global Health Authorities
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Years of Combined Clinical & Quality Experience
GCP/GxP, Vendor, Site & System Audits
Countries in Our Global Consultant Network
Regulatory & Inspection Experiences
FDA • EMA • NMPA & Global Health Authorities
OUR SERVICES
Quality Expertise for Complex Clinical Programs.
Practical quality solutions that strengthen clinical programs, systems and teams.
View All ServicesGxP Auditing
Independent GCP, GVP, GLP and GMP audits across clinical programs.
Identify the gaps before they become findings.
Critical Vendor & System Audits
Independent oversight of critical vendors, systems and endpoints.
Because critical endpoints deserve critical oversight.
Inspection Readiness
Prepare teams and programs for regulatory inspection.
See the gaps before the inspectors do.
Quality System & QMS Improvement
Build and strengthen practical, scalable quality systems.
Strengthen what works. Improve what doesn't.
Build Clinical Operations
Establish the people, processes, systems and governance for biotechs and investigator sites to run clinical trials with confidence.
Built right from the start, and built to scale.
Training & Quality Capability Building
Practical, role-based training across GCP, RBQM, CAPA, inspection readiness and complex clinical trial quality.
Build teams that know what good quality looks like.
Built to go where your
trial goes
Experienced Auditors. Wherever Your Trial Runs.
VedX brings together experienced auditors and clinical quality professionals across regions, therapeutic areas and GxP disciplines giving sponsors access to the right expertise.
No auditor network location selected.