A specialised clinical research support partner
We’re a specialized clinical research support services company dedicated to helping CROs, SMOs, and pharmaceutical sponsors accelerate trial execution, maintain regulatory compliance, and achieve operational excellence across India.
Built by Industry Veterans, For Industry Professionals
Prequel Scientific Services was founded by seasoned clinical research professionals who understood a critical challenge: CROs, SMOs, and pharmaceutical sponsors needed specialized expertise to navigate India’s complex regulatory environment and execute trials efficiently.
We saw organizations struggling with:
- Lengthy hiring cycles that delayed trial timelines
- Difficulty finding therapeutic area specialists
- Resource gaps during critical project phases
- High overhead costs of maintaining full-time teams
- Challenges navigating DCGI processes and ethics committees
Our solution was simple but powerful: become the specialized support partner that organizations could rely on—offering expert teams who integrate seamlessly, deploy rapidly, and deliver quality consistently.
Today, we’re proud to partner with leading clinical research organizations across India, providing the specialized support services that help them execute trials faster, more efficiently, and with greater quality.
Our Purpose
To accelerate clinical research in India by providing specialized support services that enable organizations to execute trials with excellence.
Our Vision
To be India’s most trusted clinical research support partner, recognized for quality, speed, and expertise.
Our Promise
Seamless integration, rapid deployment, and unwavering commitment to quality in every deliverable.
Our Core Values
The principles that guide every partnership, every project, and every deliverable.
Quality Without Compromise
Every deliverable undergoes rigorous quality review. We maintain ICH-GCP standards and documented processes to ensure inspection readiness for our partners.
Speed & Agility
We understand trial timelines are critical. Our 48-72 hour deployment model and pre-trained teams ensure you never lose momentum due to resource constraints.
Partnership Mindset
We’re not vendors—we’re partners. Our success is measured by your success, and we integrate seamlessly as an extension of your team.
Transparency & Communication
Real-time updates, open communication, and complete visibility into our work. You’ll always know exactly where things stand.
Continuous Learning
Clinical research evolves constantly. We invest in ongoing training, regulatory updates, and skill development to stay ahead of industry changes.
Excellence in Execution
Good enough isn’t good enough. We strive for excellence in every document, every submission, every data point, and every interaction.
Why Organizations Partner With Us
The Problem
Hiring specialized clinical research professionals takes 3-6 months, causing trial delays and missed milestones.
Our Solution
Pre-trained expert teams deployed in 48-72 hours, fully integrated and operational from day one.
The Problem
Maintaining full-time teams creates high fixed costs and resource underutilization between projects.
Our Solution
Flexible FSP model—pay only for work delivered, scale up or down based on your project needs.
The Problem
India’s regulatory landscape requires specialized knowledge of DCGI processes and ethics committee relationships.
Our Solution
Deep India market expertise with established processes and proven track record supporting regulatory submissions.
The Prequel Difference
- Faster Trial Startup 30-40% reduction in resource-related delays
- Cost Efficiency 40-50% savings vs. in-house hiring
- Quality Assurance 100% QC review on all deliverables
- Zero Retention Risk No employee turnover concerns
- Therapeutic Expertise Specialized knowledge across 8+ therapeutic areas
- Scalability Seamlessly scale teams based on workload
Built by Industry Veterans
Our leadership team brings decades of combined experience in clinical research, regulatory affairs, and data management across global pharmaceutical companies and leading CROs.
Our Partnership Approach
A proven methodology that ensures seamless collaboration and exceptional results.
- 01
Deep Discovery
We start by understanding your trial objectives, timelines, resource gaps, and quality requirements through detailed consultations.
- 02
Customized Team
We assemble specialists with relevant therapeutic area experience and technical expertise tailored to your specific needs.
- 03
Rapid Integration
Your team is deployed within 48-72 hours, fully onboarded, trained on your processes, and ready to contribute immediately.
- 04
Quality Execution
We deliver services with built-in quality checks, documented audit trails, and regular status updates for complete transparency.
- 05
Continuous Partnership
We provide ongoing support, flexible scaling, and proactive communication throughout your trial lifecycle and beyond.
Committed to Global Standards
Our quality management system ensures that every deliverable meets international regulatory standards and supports your inspection readiness.
ICH-GCP E6(R2) Compliance
All team members trained in Good Clinical Practice guidelines with regular refresher courses.
CDISC Standards
SDTM and ADaM implementation expertise for regulatory-compliant data deliveries.
Quality SOPs
Documented standard operating procedures for all service areas ensuring consistency.
Data Security
Secure data handling protocols and confidentiality agreements protecting client information.
Quality First
100% of deliverables undergo independent QC review before client handover
Audit Ready
Documented processes and audit trails supporting regulatory inspections
Confidentiality
Strict NDAs and data security protocols protecting your intellectual property
*Statements describe internal SOP alignment and operating practices; certificates and vendor tools are disclosed under NDA when applicable.
Ready to Partner With Us?
Discover how our specialized support services can help accelerate your clinical trials and enhance operational excellence.