Clinical ResearchExcellence
Comprehensive clinical research services across Kazakhstan's premier JCI-accredited hospital network, delivering world-class results for pharmaceutical and biotech companies worldwide.
Full-Service CRO
End-to-end clinical research services from protocol design to regulatory submission
- Protocol Development
- Site Management
- Data Management
- Regulatory Submission
Patient Recruitment
Leveraging the national healthcare database
- Database Mining
- Community Outreach
- Digital Marketing
- Site Support
Regulatory Affairs
KZ FDA submissions with data accepted by FDA and EMA
- KZ FDA Submissions
- FDA Accepted Data
- EMA Accepted Data
- Post-Market Surveillance
Ready to Start Your Clinical Trial?
Get a free feasibility assessment and discover how our expertise can accelerate your drug development timeline.
Our Proven Process
We follow a systematic approach to ensure successful clinical trial execution, from initial consultation to final regulatory submission.
Initial Consultation
1-2 weeksWe begin with a comprehensive consultation to understand your study requirements, objectives, and timeline.
Key Deliverables:
Initial Consultation
1-2 weeksWe begin with a comprehensive consultation to understand your study requirements, objectives, and timeline.
Key Deliverables:
- Study feasibility assessment
- Timeline estimation
- Budget proposal
Protocol Development
2-4 weeksOur experts develop a detailed study protocol tailored to your specific requirements and regulatory standards.
Key Deliverables:
Protocol Development
2-4 weeksOur experts develop a detailed study protocol tailored to your specific requirements and regulatory standards.
Key Deliverables:
- Draft protocol
- Regulatory strategy
- Site selection criteria
Regulatory Approval
4-8 weeksWe handle all regulatory submissions and approvals with local and international authorities.
Key Deliverables:
Regulatory Approval
4-8 weeksWe handle all regulatory submissions and approvals with local and international authorities.
Key Deliverables:
- Regulatory submissions
- Approval documentation
- Compliance certification
Site Activation
2-3 weeksWe activate and train study sites, ensuring all personnel are properly qualified and ready.
Key Deliverables:
Site Activation
2-3 weeksWe activate and train study sites, ensuring all personnel are properly qualified and ready.
Key Deliverables:
- Site training
- Equipment setup
- Quality assurance protocols
Study Execution
Study durationWe manage the entire study execution with continuous monitoring and quality control.
Key Deliverables:
Study Execution
Study durationWe manage the entire study execution with continuous monitoring and quality control.
Key Deliverables:
- Patient recruitment
- Data collection
- Quality monitoring
Data Analysis & Reporting
4-6 weeksWe analyze collected data and prepare comprehensive reports for regulatory submission.
Key Deliverables:
Data Analysis & Reporting
4-6 weeksWe analyze collected data and prepare comprehensive reports for regulatory submission.
Key Deliverables:
- Statistical analysis
- Final report
- Regulatory submission
Why Our Process Works
Faster Timelines
Our streamlined process reduces study setup time by up to 40%
Higher Success Rates
95% of our studies complete on time and within budget
Expert Support
Dedicated project managers and regulatory experts throughout
Why Choose Vantage Clinical?
We deliver measurable value through our expertise, efficiency, and commitment to excellence.
Faster Time to Market
Accelerate your drug development timeline with our efficient processes and experienced team.
Reduced study setup and execution time compared to industry average
Cost Optimization
Optimize your clinical programs with streamlined processes and strategic resource allocation.
Enhanced program efficiency through optimized clinical workflows and expert guidance
Patient Access
Access diverse patient populations through our extensive hospital network across Kazakhstan.
Large, diverse patient database across multiple therapeutic areas
Quality Assurance
Maintain the highest standards with our comprehensive quality management systems.
All hospitals maintain Joint Commission International accreditation
What Our Clients Say
"Vantage Clinical delivered exceptional results for our Phase III oncology trial. Their expertise and efficiency exceeded our expectations."
"The team's regulatory expertise and local connections made our approval process smooth and efficient. Highly recommended."
"Outstanding patient recruitment and retention rates. Their hospital network provided access to the exact patient population we needed."
Ready to Experience the Vantage Advantage?
Join the growing number of pharmaceutical companies that trust us with their clinical research needs.
Ready to Start Your Clinical Trial?
Get expert guidance and support for your clinical research project. Our team is ready to help you achieve your drug development goals.
Email Us
Send us your project details and requirements
Schedule Meeting
Book a consultation with our team
What We Can Do For You
All consultations are confidential and tailored to your specific needs.