About Us
Empowering Tomorrow's Healthcare Through Innovation and Integrity
Trial Craft Research solution was established and privately held since 2024, is a Site Management Organization (SMO) , head quartered in the location of kanchipuram, Tamil Nadu.
Trial craft SMO is exceptional in site management and project management and monitoring of phase II, III and IV clinical trials involving pharmaceutical, biological and medical device products to its clients.
Specializing in global patient recruitment, we start by accurately identifying target patient populations through feasibility and implementing cost-effective strategies and tactics to complete enrollment on time.
We have sharp business insight to address the right opportunity in the right manner and the team who is appropriately trained to execute the projects efficiently and deliver high quality on time. Our sole objective is to support the desired outcome of clinical trials.
VISION
Our vision is to charter new healthcare solutions for debilitating diseases by providing remarkable and professional site services. We believe in following the individual study protocols by remaining sticked to the four pillars of TCRS – quality, integrity, empathy and modesty.
MISSION
Our mission is to identify potential sites and educate investigators for conducting clinical trials to elevate India’s global share of conducting clinical trials. By using the technology and medical and pharmaceutical science, we aim to meet the service expectations of the Sponsors, Contract Research Organizations, and Investigators to work more effectively as a site management organization In India as well as in the entire globe.
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
immunology
infectious disease studies
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.
Our Expert Team
Furthermore, our research team is highly skilled and focused on identifying and analyzing important study data. We understand the significance of accurate and relevant data in shaping research outcomes. Our experts work closely with you to identify key metrics and ensure that the data collected is comprehensive and insightful. This collaborative approach maximizes the potential of your study and enhances the overall quality of your findings. One essential benefit of working with us is that we strive to achieve shorter study timeframes and cost-effectiveness. We understand the importance of meeting deadlines and staying within budget. Our team is equipped to efficiently monitor the study activities, compliance requirements, and closeout processes.
reach out us
If you are interested in learning more about how TCRS can support your clinical trial management needs, please feel free to reach out to us . We would be happy to schedule a call or meeting at your convenience to discuss further.
Thank you for considering Trialcraft Clinical Research Services. We look forward to the possibility of working together to advance the field of clinical research.