Strategic insights into clinical trial operations in India

ProRelix Research redefines excellence in clinical trial services in India with efficient clinical trial solutions

With a commitment to quality and innovation, we ensure every phase of your clinical research is executed seamlessly.

Proficiency in

Clinical Trial Management Services

ProRelix Research offers extensive Clinical Trial Management Services as a leading Contract Research Organization (CRO), specializing in the CRO industry with a strong focus on delivering distinguished clinical research services in India.

Our expertise spans all phases of clinical trials, ensuring that each project is managed with precision and adherence to regulatory standards. By leveraging advanced technologies and methodologies, we streamline processes, enhance patient recruitment, and maintain high-quality data management, ultimately driving successful outcomes for our clients.

Partnering with ProRelix Research means gaining access to a dedicated team committed to advancing medical innovation through efficient trial management and strategic collaboration.

Project Management

Site Management

Medical Monitoring

Vendor Management

Data Management

“Revolutionizing clinical trial approvals in India”

India’s New Drug and Clinical Trial Rules, 2019, facilitate a faster and more transparent process for obtaining clinical research approvals.

Regulatory and Ethical Prerequisites for Clinical Trials in India

Ethics Committee Registration

We assist in the seamless registration and renewal of Ethics Committees (EC) with the CDSCO through the SUGAM portal, ensuring compliance with regulatory requirements.

Clinical Trial Registry India (CTRI)

Looking to list your clinical trial on the CTRI platform? We provide expert assistance with CTRI registration and seamless submission through the official CTRI online portal. Let us simplify the process for you!

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