Iconic Peace Award
Recognised for outstanding contributions to healthcare innovation and clinical research excellence.
See the ceremonyISO 9001 · ISO 27001 India's trusted SMO & research partner
Making clinical research simpler, faster & more cost-effective
At CTRS, we're more than a service provider — we're your one-stop partner for clinical trials, regulatory affairs, market research and healthcare intelligence.
- GCP Certified Team
- 24/7 Patient Support
- FDA Compliant Research
- Advanced Data Analytics
100%Regulatory approval rate
250+Clinical trials completed
Aligned with global standards
ICH-GCP USFDA EMA CDSCO ISO 9001:2015 ISO 27001:2022 NDCT Rules 2019 21 CFR Part 11 WHO-GCLP ICH-GCP USFDA EMA CDSCO ISO 9001:2015 ISO 27001:2022 NDCT Rules 2019 21 CFR Part 11 WHO-GCLP
About CTRS
India's leading SMO delivering excellence in clinical trial research
Clinical Trial Research Services (CTRS) delivers advanced, specialised solutions in clinical trials and medical research — reflecting our passion for high-quality studies and world-class healthcare solutions.
We excel in comprehensive site management, project coordination and real-time monitoring of Phase II, III and IV clinical trials across pharmaceuticals, biologics and medical devices. Our high client retention is earned through commitment, responsiveness, adaptable service models and exceptional cost-effectiveness.
- Phase II, III & IV trial management
- Flexible, scalable engagement models
- Regulatory compliance at every step
- Seamless alignment with sponsor culture
What We Do
End-to-end solutions for healthcare innovation
From clinical trials to market research and medical writing — comprehensive services to accelerate your journey from concept to market.
Clinical Research
Site management, feasibility, recruitment and monitoring for Phase II–IV trials.
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Medical Writing
Protocols, CSRs, regulatory dossiers, safety reports and publications.
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Market Research
Primary and secondary research, KOL insights and competitive intelligence.
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CTRS Training
GCP and regulatory training plus career programs with paid internships.
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Our Clinical Research Services
Everything your study needs — under one roof
Comprehensive clinical research solutions tailored to the unique needs of your studies, helping you accelerate medical discoveries and improve patient outcomes.
01
Site Selection & Feasibility
We identify high-performing sites based on past trial data, investigator experience and patient availability — for faster enrollment and higher-quality data from day one.
02
Specialised Site Support
Our expert teams provide continuous assistance to trial sites throughout the study, improving compliance, data quality and overall trial performance.
03
Rapid Start-up
Accelerate timelines with streamlined ethics approvals and site activation — quick initiation without compromising regulatory standards.
04
Patient Recruitment & Retention
Innovative recruitment strategies to meet enrollment targets, plus retention programs that minimise dropout rates throughout the trial.
05
Overall Study Management
Comprehensive management of all trial activities with real-time monitoring and oversight to ensure timely delivery and compliance.
06
Training
World-class training for site staff on GCP, protocol-specific procedures and data collection — ensuring consistency across all sites.
How We Work
From feasibility to close-out
A proven four-stage process that keeps your study on time, on budget and inspection-ready.
Feasibility
Site identification, investigator assessment and patient-pool analysis.
Start-up
CDA, IRB/IEC submissions, contracts, budgets and site initiation.
Execution
Recruitment, CRC support, IP management, AE reporting and monitoring.
Close-out
Final documentation, data reconciliation and close-out readiness.
Therapeutic Areas
All Therapeutic Areas
Deep expertise across medical specialties
Orthopaedics
Bone, joint and musculoskeletal conditions, from arthritis to post-surgical recovery.
Oncology
Solid tumours and haematological malignancies, from targeted therapy to supportive care.
Cardiovascular
Heart and vascular disease research, from prevention to advanced procedures.
Central Nervous System
Neurological and psychiatric studies for breakthrough treatments.
Respiratory
Pulmonary diseases and respiratory conditions research.
Endocrinology & Metabolic
Diabetes, obesity and hormonal disorders.
Infectious Diseases
Bacterial, viral and parasitic infections and vaccine innovation.
Immunology & Autoimmune
Immune system and autoimmune disorder research.
Don't see your area?
We've run trials across many more specialties. Discuss your research need →
250+
Clinical Trials Completed
15+
Years of Clinical Experience
50+
Medical Research Specialists
100%
Regulatory Approval Rate
Why Choose CTRS
A client-first partner built on quality and trust
We bring the right people together, invest in long-term relationships and stand behind every engagement.
Certified quality systems
ISO 9001:2015 and ISO 27001:2022 certified operations with robust GxP practices.
Faster timelines
Quick, accurate feasibility and streamlined start-up from CDA to SIV.
Flexible engagement
Scalable support that aligns with your culture, processes and goals.
Global regulatory alignment
Processes aligned with ICH-GCP, USFDA, EMA and CDSCO requirements.
20+Clients partnered across India in two years
Message from our Founder
Read the Full Message
Our journey has been fuelled by one core belief: bringing together the right people makes all the difference. We are a client-first firm — every project is backed by our promise of quality and attention to detail. At CTRS, your success is our priority.
Ravi GuptaChief Executive Officer & Founder
Recognition
View All Achievements
Awards & achievements
Jyoti Peace Award
Honoured for exceptional service in advancing clinical research standards and patient care.
See the ceremonyExcellence in Clinical Research
Awarded for maintaining the highest standards of quality and integrity in clinical operations.
See the ceremony
Who We Serve
Trusted across the life sciences ecosystem
Pharmaceutical & Biopharma
CROs & Sponsors
Medical Devices & Diagnostics
Hospitals & Health Systems
Generics & Biosimilars
Consultants & Investors
FAQ
Questions sponsors often ask
Can't find what you're looking for? Our team is happy to help.
An SMO like CTRS manages clinical trial activities at investigator sites on behalf of sponsors and CROs — from feasibility and ethics submissions to patient recruitment, data entry and close-out — so studies run faster and stay compliant.
We provide site management, project management and monitoring for Phase II, III and IV clinical trials involving pharmaceutical, biological and medical device products.
Yes. CTRS holds ISO 9001:2015 (Quality Management Systems) and ISO 27001:2022 (Information Security Management Systems) certifications, both valid until September 2028.
Absolutely. Our processes are aligned with ICH-GCP, USFDA, EMA and CDSCO requirements, allowing us to support both Indian and international healthcare partners.
Our streamlined feasibility, ethics approval and site activation process — from CDA sign-off to Site Initiation Visit — is designed to shorten start-up timelines without compromising regulatory standards.
Ready to advance your clinical research?
Contact us today for a free consultation and let our experts help you design and implement effective clinical trials that drive your research forward.
+91-9828676917 · Mon–Fri, 9AM–6PM