Doclin Clinical Research Services is a dedicated Site Management Organization (SMO) committed to accelerating clinical trials through efficient site operations, regulatory support, and high-quality data delivery. Based in India, we collaborate with hospitals, investigators, and research sponsors to streamline clinical research processes and ensure ethical, timely, and compliant conduct of studies.
With a focus on quality, integrity, and innovation, we assist healthcare institutions in initiating and managing clinical trials by offering end-to-end support—from feasibility assessment and site setup to recruitment, monitoring, and documentation.
Our expert team brings extensive experience across multiple therapeutic areas and adheres strictly to ICH-GCP guidelines and global regulatory standards.
Vision:
To become a leading clinical research support organization recognized for excellence, transparency, and commitment to ethical research that advances medical science and improves patient outcomes.
Mission:
To deliver reliable and timely clinical trial support to hospitals, investigators, and sponsors by providing:
Seamless site management
Skilled clinical coordination
Patient-centric recruitment strategies
Quality-driven data handling
Compliance with all regulatory and ethical standards
Our Services:
Site Identification & Feasibility Support
Regulatory & Ethics Committee Submissions
Clinical Trial Site Management
Investigator Training & Support
Ethics Committee Registration
Medical Writing
Our Clients
Testimonials
Working with Doclin Clinical Research has been a game-changer for our hospital. Their team streamlined the entire clinical trial process, from documentation to patient recruitment. Their professionalism and attention to detail are truly commendable. We’ve seen significant improvements in our research timelines and data quality.
Dr. Priya Sharma, Oncologist
Doclin Clinical Research has brought exceptional value to our hospital’s clinical research operations. Their systematic approach, from managing documentation to ensuring smooth patient recruitment, has made a noticeable impact. The team’s expertise and dedication have greatly enhanced our efficiency and data accuracy.
Dr. Umer Quadri, MD Medicine
I was impressed by the efficiency and dedication of the Doclin Clinical Research team. They handled everything—from ethics committee submissions to patient follow-up—with precision and care. Their support allowed me to focus more on patient care while ensuring the trial stayed on track.
Dr. Meenal Joshi, Dermatologist
Doclin Clinical Research has been one of the most reliable and professional site management teams I’ve worked with. Their site staff is always well-prepared, documentation is audit-ready, and patient safety is given top priority. Monitoring visits are smooth because their coordination and compliance with protocols are excellent. It’s always a pleasure to work with their dedicated team.
Dr. Prasad Jadhav, Project Manager, IQVIA
Our collaboration with Doclin Clinical Research exceeded expectations. Their in-depth knowledge of regulatory requirements, strong investigator network, and commitment to high-quality data collection ensured the success of our clinical trial. Their proactive communication and problem-solving approach saved us both time and resources. We look forward to partnering with them in future studies.
Dr. Amit Joshi, CRA, PPD
Doclin Clinical Research has been an outstanding partner in our recent multi-center clinical trial. Their site management capabilities, patient retention strategies, and strict adherence to GCP guidelines played a key role in the timely completion of our study. The team is responsive, knowledgeable, and truly committed to quality research. We highly value this collaboration
Gauri Shetke, CRA, Siro Clinpharm