End to end Biometrics
Access everything – from biostatistics to data management, statistical programming and medical writing – in one place.
Save millions of dollars
and years of clinical
research time.
Better health starts with better clinical trials.
Confidently identify treatments that work better and reach patients faster with streamlined, inclusive, and technology-enabled clinical trials.
Accelerate drug development without compromising safety and quality
Boost clinical success with real-time data and predictive analytics
Simplify site operations, reduce inefficiencies, and relieve administrative burdens
Align clinical technology and solutions with real-world needs
Solutions
Advisory Services
Mitigate risks and achieve quicker results with expert guidance tailored to your goals.
Imaging Solutions
Optimize imaging data and advanced analytics to enhance trial outcomes.
Patient Access & Site Solutions
Streamline patient recruitment, simplify site management, and automate compliance without additional burdens.
CELLTROVE FOR
Biopharma
Quickly deliver life-changing therapies to patients. Streamline trials, reduce costs, and accelerate drug development with a technology-enabled, expert-led clinical research ecosystem.
THE OPPORTUNITY
Launch new therapies in double quick time, at half the cost.
Save millions in clinical research costs with a single-window digital workflow that takes researchers from data to decisions in minutes.
Improve predictive accuracy of clinical success by 80%-89% with ML-powered analytics.
THE OPPORTUNITY
Win more sponsor contracts with 50% faster, automated and efficient trials.
Save months of study time and millions in costs by accessing global talent and large patient populations.
Improve approval rates with high quality regulatory-ready data packages.
Prioritize high-performing trial sites with real-time analytics on geographic, demographic, and infrastructure data.
CELLTROVE FOR
CROs
Expand into multiple markets and geographies with minimum risks and overheads. Maximize operational efficiency with global talent and data-driven digital clinical research solutions.
CELLTROVE FOR
Clinical Technology Providers
Co-develop intuitive, interoperable, and impactful solutions grounded in clinical realities. Reduce inefficiencies, integrate your innovation with existing trial platforms, and unlock its full potential with our insider knowledge.
THE OPPORTUNITY
Build smarter, automated and, more adoptable clinical trial solutions using AI/ML/NLP.
Reduce efforts on repetitive task with consistent quality outputs.
Relieve user burden with intuitive technology solutions that address real-world needs.
THE OPPORTUNITY
Save years of manual work by streamlining 80% of clinical study workflows.
Manage multiple trials from recruitment to reporting - on a single platform.
Axe patient recruitment workload by 90% and start studies faster.
Reduce revenue leakage and improve cash flow with automated payments system.
CELLTROVE FOR
Clinical Site Investigators
Relieve administrative and compliance burdens with automated data capture and reporting. Maintain high-quality data with real-time centralized monitoring. Improve recruitment and retention with patient-centric clinical trials.
Expertise you can trust
Bhavesh Acharya
Founder & Director
Celltrove is led by Bhavesh Acharya, a clinical development leader with over 25 years of experience across Clinical Operations, Clinical Data Management / Biostatistics, and Clinical Trial Site Solutions in India and China. Bhavesh has
- established and led the first Pharma-CRO FSP collaboration center in Bengaluru, India
- set up multiple Center of Excellence delivery centers for major US based pharmaceutical companies and Clinical Research Organizations
- conceptualised Site Solutions Model to provide support to Clinical Trial Sites
- .established and led the first Pharma-CRO FSP collaboration center in Bengaluru, India
- .set up multiple Center of Excellence delivery centers for major US based pharmaceutical companies and Clinical Research Organizations
- .conceptualised Site Solutions Model to provide support to Clinical Trial Sites
Bhavesh is a pharmacist by education and he is also trained at IIM Ahmedabad (India) and Forum Corporation (USA) on building Strategies, Leadership, and Coaching. He is a global speaker and has presented and participated in various conferences across India and overseas at forums such as SCDM (Member, Active Speaker & India Chair 2025), PHUSE (Active speaker), ISCR (Lifetime Member & Scientific Committee Chair – 2022, 2023 & 2024), DIA & China Clinical Trials.
