Neuheit Research, an associate entity of Neuheit Services LLP, is a full-service Clinical Research Organization (CRO) delivering compliant, ethical, and high-quality clinical research services across India.
We partner with pharmaceutical companies, biotechnology firms, investigators, hospitals, and research institutions to support end-to-end execution of clinical trials across diverse therapeutic domains.
With a foundation in scientific rigor, regulatory excellence, and quality-driven processes, Neuheit Research ensures data integrity, patient safety, and consistent delivery throughout the clinical research lifecycle.
Dr Souraabh Ambapkar
Founder
Comprehensive Clinical Trial Management
End-to-end support
Regulatory & Ethical Compliance
Strict adherence to ICH-GCP guidelines, ethics committee approvals, and global regulatory standards
12 Years Experience
Our Mission
To support the development of safe and effective therapies by delivering clinical research services with integrity, operational excellence, and a patient-centric approach.
To deliver ethical, high-quality, and compliant clinical research solutions that advances the healthcare.
To ensure data integrity through scientific excellence and transparent collaboration.
Our Vision
To be a trusted and preferred Clinical Research Organization, setting industry benchmarks in quality, Operational excellence, regulatory compliance, ethical contributions to clinical research across diverse therapeutic areas and patient-centric healthcare.
16 +
Specialized center
in 16 states
1 k
Material Collection
points
172
Patients diagnosed
2019
112 +
Specialized center
in 16 states
Our Core Values
Our core values define our commitment to
ethics, quality, and patient-centric research.
Integrity
We uphold the highest standards of honesty, transparency, and ethical conduct in all aspects of clinical research.
Quality Excellence
We are committed to delivering accurate, reliable, and reproducible data through robust systems, standardized processes, and continuous quality improvement.
Patient-Centricity
We place patient safety, rights, and well-being at the forefront of every clinical study we support.
Regulatory Compliance
We operate in strict adherence to ICH-GCP, CDSCO, and all applicable national and international regulatory requirements.
Collaboration
We work collaboratively with sponsors, investigators, healthcare institutions, and partners to achieve shared scientific and operational objectives.
Accountability
We take full responsibility for our commitments and deliver with consistency, professionalism, and operational discipline.
Our Clinical Trial Execution Framework
We follow a structured, end-to-end approach to clinical research that ensures clarity, efficiency, and regulatory compliance at every stage—from study planning to final delivery of results.
Define the Study
Clear understanding of objectives, protocol, timelines, and regulatory requirements to establish a well-defined project scope.
Design the Solution
Customized clinical strategy including feasibility, site selection, budgeting, and regulatory planning tailored to study needs.
Execute the Trial
Comprehensive management of site initiation, patient recruitment, monitoring, data collection, and quality oversight.
Deliver Results
Accurate data validation, timely reporting, safety submissions, and successful study close-out in full regulatory compliance.
testimonials
Some feedbacks from
honorable clients
700 +
Satisfied Users Over the Global
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