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 CDSCO 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 support clinical research organisations across India, providing the specialised services that help them execute trials efficiently and to standard.
Our Purpose
To accelerate clinical research in India by providing specialized support services that enable organizations to execute trials with excellence.
Our Vision
To become a clinical research support partner our clients return to, on the strength of quality, responsiveness 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
Deliverables go through documented quality review before handover. We work to ICH-GCP and documented processes that support our partners’ inspection readiness.
Speed & Agility
We understand trial timelines are critical. Because teams are pre-trained and deployed to an agreed schedule, resourcing is less likely to become the thing that holds a study up.
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
Regular status updates, open communication and clear visibility of progress, at the cadence agreed in your work order.
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 specialised clinical research professionals takes months, causing trial delays and missed milestones.
Our Solution
Pre-trained expert teams deployed to an agreed timeline, integrated and operational from the start.
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 CDSCO processes and ethics committee requirements.
Our Solution
Deep India market expertise with established processes and direct experience supporting regulatory submissions.
The Prequel Difference
- Faster Trial Startup Pre-trained teams take the hiring cycle off your critical path
- Cost Efficiency Pay for work done rather than carrying permanent headcount
- Quality Assurance Independent QC review built into our delivery process
- Continuity of Cover Backup cover and handover planning, so staff changes are managed by us
- Therapeutic Expertise Experience across oncology, rare disease, devices and post-marketing safety
- Scalability Seamlessly scale teams based on workload
Our Leadership Team
Our leadership team brings combined experience in clinical research, regulatory affairs and data management, from global pharmaceutical companies and CROs.
Our Partnership Approach
A structured way of working that keeps collaboration clear from first conversation to closeout.
- 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 to the timeline agreed in your work order, onboarded, trained on your processes and ready to contribute.
- 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 is designed so that deliverables meet the applicable regulatory standards and support your inspection readiness.
ICH-GCP E6(R3) Aligned
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
Independent QC review built into delivery, 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.