Supporting Innovation at Every Stage
Integrated scientific services supporting the development, safety assessment and regulatory progression of pharmaceuticals, biologics, medical devices, specialty chemicals, cosmetics and other regulated products.
Science that supports confident decisions
Adgyl Lifesciences, in collaboration with its laboratory partner, Eurofins India, provides integrated scientific services that support the development and safety assessment of pharmaceuticals, biologics, medical devices, specialty chemicals, cosmetics, and other regulated products.
By combining expertise in pharmacology, toxicology, bioanalysis and specialised safety evaluation , we help organisations generate reliable data and advance products with confidence.
Integrated support across the development journey
From early discovery through regulatory preparation, our capabilities connect scientific expertise with development milestones.
Discovery
Explore targets and identify promising opportunities.
Pharmacology
Generate evidence through in vitro and in vivo studies.
DMPK & Bioanalysis
Characterise exposure, metabolism and biological response.
Safety
Generate critical safety and toxicology data.
Regulatory
Support IND-enabling studies and NDA filing requirements.
Integrated scientific expertise
Our capabilities span discovery, pharmacology, toxicology, bioanalysis and regulatory development support.
Discovery Chemistry
Scientific support across early discovery and chemistry-led development programs.
Explore →Pharmacology & Imaging
In vitro, in vivo pharmacology and in vivo imaging solutions supporting development programs.
Explore →DMPK
Drug metabolism and pharmacokinetic studies supporting compound characterisation and development.
Explore →In Vitro Toxicology
In vitro approaches supporting the evaluation of potential safety risks.
Explore →Exploratory Toxicology
Exploratory toxicology studies designed to generate critical development insights.
Explore →Genetic Toxicology
Genetic toxicology studies supporting safety evaluation and development decisions.
Explore →Safety Pharmacology
Studies supporting assessment of potential effects on critical physiological systems.
Explore →Developmental & Reproductive Toxicology
DART studies supporting developmental and reproductive safety assessment.
Explore →Inhalation Toxicity
Specialised inhalation toxicity studies supporting product safety assessment.
Explore →Bioanalytical Services
Bioanalytical support for reliable data generation across development programs.
Explore →IND-Enabling Studies
Integrated studies supporting preparation for investigational new drug submissions.
Explore →NDA Filing
Scientific support for data packages and requirements associated with NDA filing.
Explore →Biologics
Scientific capabilities supporting the development and assessment of biologic products.
Explore →Built to support confident decisions
Integrated expertise helps organisations accelerate development, reduce risk and generate the data needed for critical decisions.
Clients supported
Years of drug development experience
Investigational New Drug packages submitted
A scientific partner through every milestone
Scientific Rigor
Reliable scientific data generated through integrated expertise and specialised capabilities.
Integrated Expertise
Connected capabilities spanning discovery, pharmacology, toxicology and bioanalysis.
Development Confidence
Generate the evidence needed to advance products and support critical development decisions.
Looking for a trusted scientific partner?
Our integrated capabilities help accelerate development, reduce risk and generate the data needed to make critical decisions with confidence.