About Us
VCLINICAL is a premier Contract Research Organization (CRO) dedicated to delivering end-to-end clinical development solutions. With decades of combined expertise, our multidisciplinary team partners with biotech, pharmaceutical, and medical device innovators to bring safe and effective products to market faster.
Our Mission
To empower sponsors with agile, high-quality, and cost-effective clinical research services—transforming scientific vision into life-changing therapies.
Holistic Expertise
From First-in-Human to Phase IV, our seasoned clinicians, statisticians, and regulatory specialists guide every stage of your trial.
Tailored Solutions
We design bespoke study protocols and operational plans that align with your strategic objectives, ensuring efficient resource utilization.
Global Reach, Local Insight
Operating across North America, Europe, and Asia Pacific, we blend global infrastructure with on-the-ground knowledge to navigate regional regulations seamlessly.
Data-Driven Decisions
Our robust eClinical platform delivers real-time analytics, enabling proactive risk management and transparent study oversight.
Regulatory Excellence
VCLINICAL’s regulatory affairs team maintains close relationships with health authorities worldwide, streamlining submissions and accelerating approvals.
Clinical Trial Management
• Protocol development & feasibility
• Site identification & activation
• Patient recruitment & retention
• Monitoring & quality assurance
Regulatory Affairs
• IND/CTA submissions
• Regulatory strategy & consulting
• Labeling & post-approval commitments
Biostatistics & Data Management
• Statistical analysis plans
• Data capture & coding
• Integrated reporting & visualization
Medical Writing
• Clinical study reports (CSRs)
• Investigator brochures (IBs)
• Regulatory dossiers & publications
Pharmacovigilance
• Safety monitoring & signal detection
• Aggregate safety reporting
• Risk management planning
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