About Us
Research
About Curaclin Research
We are a Site Management Organization, established in 2022 ,with our headquarters in Cuttack. With an ISO 2015-2019 accreditation and registered with Dun & Bradstreet under FDA guidelines, we are positioned to provide extensive clinical research services across various sites in India. With the accredited and registered status, we can guarantee quality and compliance at all levels which makes us a reliable outsourcing partner for full scope of clinical research operations.
Strength
Our Strength
We are the only professionally organised entity in India that specializes in site management for clinical research. If you have a trial or study that needs to be conducted seamlessly, you can reach out to us and we will handle it. We have partnerships with 15 multi-speciality hospitals, providing access to over 1700 hospital beds.
Our capabilities extend to conducting studies in all indications, and our team at Curaclin Research has successfully acted as a rescue site for numerous multicentric trials with eminent sponsors. We strictly adhere to the guidelines set by the Drug Controller General of India (DCGI) and are deeply committed to maintaining high quality standards.
Our innovative team model for site management includes various roles such as Centre Manager, Site Coordinator, Medical Coordinators, Quality Manager, and Research Coordinators. Together, they ensure efficient operations and seamless execution of clinical trials.
With over 11 successful clinical studies and trials conducted for leading Indian Pharma companies and reputed Pharma MNCs, we have established ourselves as a reliable name in Eastern India. Our track record demonstrates our ability to conduct clinical trials efficiently while maintaining full compliance with regulatory norms.
“
Paving the way to clinical research in India
All studies conducted at Curaclin Research are performed in accordance with Good Clinical Practice guidelines (ICH & GCP) and federal regulations.
All of our studies that we participate in are approved by an IRB – Institutional Review Board & IEC. According to New Drug and Clinical Trial Rules, 2019,
India promotes faster and transparent approval processes for Clinical Research.
Benefits
Benefits of working with Us
Curaclin Research partners with Sponsors and CROs to optimize site management and enable hospitals to establish Clinical Research Departments for successful trials.
Our approach to attracting and retaining patients is more efficient, leveraging networks of qualified patient pools and ensuring prompt follow-up.
Our research team prioritizes data cleaning over interpretation, addressing a common pitfall in clinical research to enhance overall focus and effectiveness.
We proactively mitigate delays associated with study and regulatory data by employing advanced technology infrastructure and robust data handling systems for both clinical and regulatory needs.
We provide comprehensive clinical trial services, from initiation to monitoring and closeout, which expedites research timelines while maintaining budgetary constraints, resulting in shorter study durations and reduced costs.
Navigating the complex regulatory environment is challenging for clinical trials. Site Management Organizations (SMOs) provide expertise in regulatory compliance, ensuring adherence to guidelines and minimizing the risk of violations.
With the adoption of CTMS, the activity of invoicing, communication, and collaboration is organized in a manner that improves the effectiveness and efficiency of clinical trials.
Testimonials
What Our Partners Say!
Our commitment to clinical research excellence is reflected in the feedback we receive from our esteemed clients in hospitals, clinics, and medical organizations.
Our partners in healthcare trust Curaclin Research for clinical excellence. Learn more about our services.
