Comprehensive clinical & research solutions
CTRS provides end-to-end solutions across clinical operations, market research and healthcare intelligence — helping life sciences teams accelerate development, optimise strategies and deliver measurable impact.
Everything you need, from protocol to market
From clinical trials to market research and medical writing — comprehensive services to accelerate your healthcare innovation journey.
Clinical Trial Services
End-to-end clinical trial management with expert site management and regulatory compliance.
- Site identification & feasibility
- IRB/IEC submissions, contracts & budgets
- Investigator training & site SOP development
- Patient recruitment & retention
- Clinical Research Coordinator (CRC) support
- Monitoring, SDV & EDC support
Market & Primary Research
Real-time market intelligence through expert insights and comprehensive surveys.
- KOL interviews & expert insights
- Competitive and launch intelligence
- Market sizing and forecasting
- Price and market access surveys
- Prescription trends and adoption studies
- 10-year forecasts and epidemiology views
Secondary Research & Analytics
Comprehensive literature analysis and market intelligence reports.
- Literature reviews & landscape scans
- Clinical pipeline & trial analysis
- Patent and policy landscapes
- Therapy MoA & API assessments
- Sales analytics & brand tracking
- Dashboard creation for decision support
Quality & Compliance
Comprehensive audit and quality assurance services ensuring regulatory alignment.
- GCP/GLP compliance audits & vendor qualification
- Site and facility audits
- TMF review and protocol verification
- Mock inspections (DCGI/USFDA/EMA)
- CAPA design & inspection support
Medical Writing
Comprehensive medical writing services across clinical development and regulatory submissions.
- Protocols, IBs, CSRs
- IND/NDA/MAA/CTA submissions
- Safety reports (DSUR, PBRER/PSUR, PADER)
- Risk Management Plans
- Manuscripts, posters & regulatory white papers
More ways we support your programme
CSV Services
Risk-based computer system validation for EDC, CTMS, LIMS and other GxP systems.
Learn moreHerbal Research
Evidence, safety and clinical studies for herbal, botanical and AYUSH products.
Learn moreMedical Coding
MedDRA and WHODrug coding for trials, plus certification-focused coding training.
Learn moreQuality & Compliance
GCP/GLP audits, TMF reviews, CAPA planning and regulatory inspection readiness.
Learn moreCTRS Training
GCP, NDCT and US FDA training for Ethics Committees, plus career programs for graduates.
Learn moreTherapeutic Areas
Specialised expertise across 15+ therapeutic areas and medical specialties.
Learn moreAlso available on request
Tailored support for every stage of drug development, delivered with partner specialists where needed.
Ready to accelerate your healthcare innovation?
Partner with CTRS for evidence-based clinical research and market intelligence solutions that deliver measurable impact.
+91-9828676917 · Mon–Fri, 9AM–6PM