Clinical Trial Registry of India

CTRI

Ensure regulatory compliance and streamlined registration for your clinical trials on CTRI with our dedicated support.

We provide end-to-end support for registering clinical studies with the CTRI, ensuring compliance with regulatory requirements and enhancing the visibility of your research. Proper registration is crucial for promoting transparency, accountability, and credibility in clinical research.

Our Services Include:

Comprehensive Guidance

Creating your CTRI account, assistance with preparing and verifying all required documentation, ensuring your study meets CTRI’s guidelines.

Protocol Review

Thorough review of your study protocol to ensure alignment with CTRI’s mandatory fields and requirements.

Data Entry and Submission

Accurate data entry on the CTRI platform and timely submission to facilitate smooth approval.

Compliance Support

Ensuring adherence to ICMR, NDCT 2019, and international clinical trial standards during the registration process

Why Choose Us?

Expertise in navigating CTRI processes for investigator-initiated and sponsored trials.
Efficient and hassle-free service to save time and resources.

Let us handle the complexities of CTRI registration so you can focus on conducting impactful research. Contact us today to get started!

Note: We prioritize the confidentiality and security of our customers’ data above all else. To ensure the highest level of trust and protection, we will first sign a formal confidentiality agreement with you. Only after this agreement is in place will we request the necessary information, ensuring that the confidentiality and integrity of your documents are fully safeguarded.

Medical Writing

Accreditation

Regulatory Approvals

On Site

Clinical Research Courses

Training Modules