Welcome to
KV Clinical Research
(Site Development & Management Organization)
Who we are
KV Clinical Research (KVCR), established in 2015, is the first Site Development & Management Organization (SDMO) in Chhattisgarh, India. We advance life-changing therapies and medical technologies through scientific, biomedical, and clinical research. By collaborating with pharmaceutical companies, laboratories, medical device manufacturers and hospitals, we deliver ISO-standard quality data in a cost-effective manner. With an experienced team and a strong hospital network across different regions of India, we conduct research in diverse populations and localities, generating broader, more reliable and impactful data outcomes. Our commitment to excellence drives scientific innovation and supports breakthrough therapeutic solutions for patients who need them most.KV Clinical Research (KVCR), established in 2015, is the first Site Development & Management Organization (SDMO) in Chhattisgarh, India. We advance life-changing therapies and medical technologies through scientific, biomedical, and clinical research. By collaborating with pharmaceutical companies, laboratories, medical device manufacturers and hospitals, we deliver ISO-standard quality data in a cost-effective manner. With an experienced team and a strong hospital network across different regions of India, we conduct research in diverse populations and localities, generating broader, more reliable and impactful data outcomes. Our commitment to excellence drives scientific innovation and supports breakthrough therapeutic solutions for patients who need them most.
OUR SERVICES
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What We Do?
Site Development & Management
KV Clinical Research (KVCR) is a leading Site Development & Management Organization dedicated to establishing new clinical research sites in partnership with hospitals. We also manage and strengthen existing research sites to ensure smooth, compliant, and efficient execution of clinical trials across Phase I–IV, PK, and BA/BE.
Training & Compliance Programs
We conduct specialized training programs on ICH-GCP, NDCT Rules, and other essential regulatory guidelines required for clinical and biomedical research. These programs are designed for all professionals directly or indirectly involved in research activities to maintain quality, ethics, and compliance standards.
Collaboration with CROs
KVCR partners with Contract Research Organizations (CROs) to support the successful planning, coordination, and execution of clinical trials. Our expertise helps CROs achieve efficient site operations, quality data collection, and timely study completion.
Partnership with Sponsors
We collaborate with study sponsors to facilitate end-to-end clinical trial execution, ensuring regulatory compliance, operational efficiency, and reliable outcomes. Our strong site network helps sponsors reach diverse patient populations across India.
Laboratory Collaborations
We work with NABL-accredited laboratories for all research-related diagnostic and pathological testing. This ensures accurate, high-quality, and dependable results that support successful clinical and biomedical research studies.
OUR NETWORK
KV Clinical Research operates a strong nationwide network of more than 35 cities across India, enabling efficient, accessible, and high-quality service delivery. Our presence includes Kolkata, Delhi, Deoghar, Dehradun, Ludhiana, Chandigarh, Patna, Bhubaneswar, Ranchi, Nagpur, Indore, Chennai, Ahmedabad, Guwahati, Bangalore, Vadodara, and Raipur. Our head office is located in Raipur, Chhattisgarh, from where all operations are centrally managed and coordinated. This extensive network allows KV Clinical Research to address diverse regional needs while maintaining consistency, operational excellence, and seamless collaboration across all sites, ensuring reliable outcomes and strong local engagement nationwide.
OUR LEADERS
DR. KIRTI KUMAR PATEL
B. Pharm., M. Sc. (Clinical Research), MBA (Operation Management), PGPM (Sales & Digital Marketing), Ph.D. (Pharmaceutical Science)
He is the only professional in Chhattisgarh holding an M.Sc. in Clinical Research along with a Ph.D. in Pharmaceutical Science. With over 10 years of experience in clinical research, he has expertise in site development, regulatory compliance, ethics processes, and clinical trial management. He plays a key role in strengthening research infrastructure and advancing quality clinical studies.
Dr. Vikas R Chandrakar
Pharm. D, Ph.D. (Pharmaceutical Science), MBA
He has more than 12 years of experience in clinical research and trial management. He brings strong scientific, operational, and project management expertise in coordinating studies, ensuring compliance, and maintaining high research standards. His experience supports the successful execution of complex clinical projects.
ADVISORY PANEL
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