About TrialCraft

Trialcraft Clinical Research Services Pvt. Ltd.

Trialcraft Clinical Research Services Pvt. Ltd. offers comprehensive end-to-end clinical trial and site management services tailored for Contract Research Organizations (CROs), pharmaceutical companies, biotechnology firms, and medical device companies.

At Trialcraft, we are committed to advancing medical research and enhancing patient outcomes through our extensive range of clinical trial services

Our experienced team provides a full suite of services, including protocol development, site management, data analysis, and quality assurance. We ensure that every trial is conducted with the utmost integrity and compliance with industry standards.

Our dedication to quality and strict adherence to Good Clinical Practice (GCP) guidelines instills confidence in our clients regarding the integrity of the data we collect and the safety of the participants involved.

We invite you to discover how Trialcraft can support your clinical research needs and facilitate the development of innovative therapies. Contact us today to learn more!

Our Vision

To be a trusted partner in clinical research, dedicated to advancing medical knowledge and enhancing the quality of life for patients around the world. We aim to change the clinical research landscape by promoting collaboration, integrity, and quality, ultimately leading to better patient outcomes and progress in medical science.

Our Mission

Our mission is to offer complete clinical trial services that adhere to the highest quality and compliance standards. We prioritize the safety and well-being of participants while providing reliable data to our clients. We are committed to driving innovation, maintaining strong ethical standards, and contributing to the advancement of healthcare.

Markets We Engage With

research and development
phase 1-4 clinical trials
bioavailability/bioequivalence (PK) studies
herbal and ayurvedic research
allopathy studies
oncology and cardiology research
homeopathy trials
medical devices research
Infectious disease studies
Immunology

What are the benefits

We understand the importance of well-organized administrative processes in compliance with regulatory affairs. By partnering with TCRS, our clients benefit from our expertise and meticulous attention to detail, ensuring a seamless experience throughout the clinical trial process.


  • Expert Guidance : Experienced professionals ensure compliance and best practices.
  • Cost Efficiency : Streamlined processes save money and maximize investment.
  • Accelerated Timelines : Projects move faster, getting products to market ahead.
  • Strategic Insights : Data analysis drives informed decision-making.

The Visionary Leader

Dr. Priya Rajendran's Vision for Clinical Excellence

Dr. Priya Rajendran, our Founder and Director, didn't just start a CRO—she set out to fix a broken system. With an MBBS and MD in Pharmacology, her career began at the research frontline as a Principal Investigator, where she experienced firsthand the delays and inefficiencies that plague clinical trials.

This hands-on insight is the foundation of Trialcraft. She envisioned a new model: one that leverages technology and deep site relationships to eliminate the bottlenecks she once faced. Under her leadership, Trialcraft is not just managing trials; we are reengineering them for speed, quality, and predictability.

Her direct experience in conducting 50+ clinical studies is the reason why our strategies are pragmatic, our processes are site-friendly, and our commitment to data integrity is non-negotiable.


Our Expert Team - The Pillars Version

Our team is built on three core pillars:

  1. Depth of Experience: Our team includes former PIs, CRAs, and data managers from top institutions, with direct experience in over 50+ clinical trials across oncology, cardiology, and endocrinology.
  2. Operational Excellence: We don't just have individual experts; we have a team that excels at integrated execution. Our project management ensures seamless collaboration between monitoring, data and regulatory functions.
  3. Commitment to Compliance: Every team member is rigorously trained in GCP and regulatory standards, ensuring data integrity and participant safety are never compromised. We build quality into every step of the process.