Your partner in clinical research success
From feasibility to close-out, we deliver comprehensive clinical trial management solutions tailored to your unique needs.
Study start-up made smoother and more affordable
Starting a new clinical study often comes with tight timelines, high costs and complex requirements.
At CTRS, we make this process smoother and more affordable by tailoring our solutions to the unique needs of every sponsor — from CDA sign-off all the way to the Site Initiation Visit.
Comprehensive services covering every aspect of execution
Study Staff Training
We appoint experienced CRCs and study managers, and all site staff receive GCP and study-specific training to maintain the highest compliance standards.
Site SOP Preparation
GCP-compliant, site-specific SOPs tailored to support the flawless execution of your trial.
Feasibility Assessment
We identify the most suitable sites and investigators, conduct feasibility studies and support site initiation.
IRB/IEC Support
Faster submissions and approvals from Institutional Review Boards and Ethics Committees to keep you on schedule.
Contract & Budget Assistance
We simplify site contracts, cost analysis and budget negotiations — saving time and ensuring financial transparency.
Subject Recruitment & Retention
From screening to enrolment, our CRCs drive faster recruitment while prioritising retention and follow-ups.
Informed Consent Process
We guide participants through consent with care and clarity, ensuring they fully understand their role.
Patient Care
Participant safety and comfort are our top priority, with continuous support throughout the trial.
Drug Dispensing & Accountability
IP storage, dispensing, documentation, returns and destruction managed with precision.
Adverse Event Reporting
Timely detection, recording and reporting of adverse events for patient safety and compliance.
Case Report Forms (CRFs)
Expertise in paper and EDC — ensuring accurate, high-quality CRF completion and maintenance.
Site Master File Maintenance
Organisation and completion of essential study documents, making compliance stress-free.
Monitoring & Auditing
Frequent internal monitoring minimises protocol deviations and keeps trials running smoothly.
IP Management
From temperature logs to shipment, retrieval and destruction — end-to-end IP handling.
Study Close-Out
Support through final recruitment, documentation and close-out readiness.
A structured path from feasibility to close-out
Feasibility & Site Selection
Data-driven site and investigator identification.
Regulatory & Start-up
IRB/IEC, contracts, budgets and SIV.
Recruitment & Conduct
CRC support, consent, patient care and IP.
Monitoring & Close-out
QC, AE reporting, SMF and close-out.
Trials across 15+ therapeutic areas
Our clinical research expertise spans diverse medical specialties, from oncology and cardiology to rare diseases and paediatrics.
Explore Therapeutic AreasOrthopaedics
Oncology
Cardiovascular
Central Nervous System
Respiratory
Endocrinology & Metabolic
Infectious Diseases
Immunology & Autoimmune
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