Clinical Research Services
CTRS – 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 Services at CTRS
Starting a new clinical study often comes with challenges—tight timelines, high costs, and complex requirements.
At CTRS, we make this process smoother and more affordable by tailoring our solutions to fit the unique needs of every sponsor.
200+ Studies
Successfully managed feasibility assessments
Faster Timelines
Quick and accurate feasibility assessments
Full Support
From CDA sign-off to Site Initiation Visit
How We Support Your Trials?
Comprehensive services covering every aspect of clinical trial execution.
Study Staff Training
We appoint experienced CRCs and study managers to ensure trials run smoothly. All site staff receive GCP and study-specific training from our experts to maintain the highest compliance standards.
Site SOP Preparation
Every site needs clear, compliant processes. We prepare 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—ensuring that your study begins on the right foundation.
IRB/IEC Support
Our team assists with faster submissions and approvals from Institutional Review Boards/Ethics Committees, helping you stay on schedule.
Contract & Budget Assistance
We simplify site contracts, cost analysis, and budget negotiations, saving you time and ensuring financial transparency.
Subject Recruitment & Retention
From screening to enrolment, our CRCs help achieve faster recruitment while prioritizing subject retention and follow-ups, ensuring study success.
Informed Consent Process
We guide participants through the consent process with care and clarity, ensuring they fully understand their role before joining a study.
Patient Care
The safety and comfort of participants are our top priority. Our study staff provide continuous support and care throughout the trial.
Drug Dispensing & Accountability
We manage IP storage, dispensing, documentation, returns, and destruction with precision, ensuring compliance at every step.
Adverse Event Reporting
Our team ensures timely detection, recording, and reporting of adverse events, supporting patient safety and regulatory compliance.
Case Report Forms (CRFs)
With expertise in both paper and electronic data capture (EDC), our CRCs ensure accurate, high-quality CRF completion and maintenance.
Site Master File Maintenance
We handle the organization and completion of essential study documents, making compliance stress-free for your site team.
Monitoring & Auditing
Frequent internal monitoring helps us minimize protocol deviations and ensure trials run smoothly from start to finish
Investigational Product (IP) Management
From temperature logs to shipment, retrieval, and destruction, we take care of end-to-end IP handling.
Study Close-Out
We support sites through final recruitment, documentation, and close-out readiness, ensuring everything is complete before sponsor or CRO review.
Why Work With CTRS Clinical Research?
We’re more than a service provider—we’re your partner in making clinical research simpler, faster, and more cost-effective.
We simplify processes and help you achieve more in less time—without inflating costs.
Our dedicated, well-trained CRCs provide hands-on site support.
Every project is backed by strong project management and quality commitment.
We add value with extra services at no hidden cost.
Protocols and site SOPs are followed diligently
Flexible and transparent pricing tailored to your needs.
A dedicated team assigned based on your project’s scope.
Master Services Agreements available to streamline multiple projects.
You get direct access to our customer support team from Day 1
We see ourselves as an extension of your team, not just a service provider.
Our Expertise in Clinical Project Management
Clinical trials demand precise planning and coordination, and that’s where our expertise makes the difference. At CTRS, we don’t just track timelines—we align every step with your study’s bigger goals.
Our project managers are hands-on, proactive, and adaptive, ensuring trials are conducted efficiently, safely, and within budget. We thrive on solving challenges and keeping your study on course.
By combining strong supervision, smooth coordination, and clear communication, we help transform your vision into a successful clinical outcome.
The CTRS Advantage
Choosing the right partner can make all the difference in the success of a clinical trial
Faster Timelines
Quick patient enrolment, rapid query resolution, and faster site initiations, ensuring your study moves forward without delays.
Flexible Approach
We adapt our internal processes to meet the unique needs of each sponsor, offering the agility and responsiveness required.
Cost-Effective Solutions
Through project-specific efficiencies, we help reduce overall study costs without compromising outcomes.
Expertise You Can Trust
Our team combines deep therapeutic area knowledge with continuous training, ensuring expertise across a wide range of clinical domains.
Our Sites
Wide network across major cities in India