Dedicated to bridging the gap between innovative scientific hypotheses and validated clinical translation through cutting-edge laboratory infrastructure.
Unitech Research Solutions (URS) was established in Pune, Maharashtra, as a premier Contract Research Organization (CRO) committed to empowering pharmaceutical manufacturers, biotechnology ventures, phytomedicine innovators, and academic researchers.
We operate an integrated laboratory suite designed to execute high-precision preclinical pharmacology, in-vitro cytotoxicity and apoptosis assays, analytical HPLC/HPTLC method development, histopathological scoring, and computational drug discovery under one unified roof.
Our mission is driven by a deep conviction: true scientific progress demands uncompromising accuracy, full data traceability, and ethical research protocols.
"Our goal is not merely to perform laboratory testing, but to generate verifiable scientific insights that accelerate global therapeutics."
The ethical and scientific pillars that govern every protocol, experiment, and technical dossier at URS.
To be recognized globally as the most trusted and innovative contract research partner, known for accelerating translational drug discovery, maintaining impeccable data integrity, and fostering scientific advancement across academia and industry.
To provide world-class, GLP-compliant preclinical, analytical, and cell-based research services with rapid turnaround times, transparent communication, and comprehensive documentation that empowers clients to achieve regulatory approvals and high-impact publications.
How URS ensures that every data point, chromatogram, and histology slide withstands international regulatory and journal scrutiny.
All in-vivo studies comply strictly with CPCSEA guidelines and ethical clearances. Calibration protocols adhere to National Accreditation Board benchmarks.
We deliver unadulterated raw chromatographic peak files, spectrophotometer absorbance values, digital photomicrographs, and audit trails alongside summary charts.
Proprietary botanical fractions, synthetic lead molecules, and formulation matrices are treated with strict confidentiality under legally binding non-disclosure agreements.
Research Requirement → Study Design → Experimental Execution → Data Analysis → Documentation → Technical Report
Dedicated leadership bringing decades of combined expertise in pharmacology, formulation science, and analytical chemistry.
Leading expert in pharmaceutical research with extensive experience in formulation development and analytical testing. Passionate about driving quality in clinical research.
