Analytical Research & Development

GLP Certified lab from National GLP compliance Monitoring Authority. Following service are provided by the department:

Technical Expertise

  • HPLC
  • AAS
  • GC
  • FTIR, UV
  • Stability indicating assay methods
  • Method development and validation


  • IP, BP, USP analytical testing
  • Method transfer
  • Finished product
  • Herbal products
  • Elemental analysis
  • Quality compliance
  • Bioanalysis

Cell Culture & Molecular Biology

Mechanism till Molecular Levels

Technical Expertise

  • Western, Northern, and Southern blotting
  • PCR
  • Cell imaging
  • Cell culture (primary cultures/Hybridoma cultures)
  • High throughput assays


  • Gene expression studies
  • Cell biochemistry
  • Immunoblotting
  • Genotoxicity studies
  • Cell transfection studies
  • Protein knock down studies
  • Ligand binding studies


  • MIC, MBC, MPC, MBEC AST determinations
  • Time kill curve studies & Breakpoint determinations
  • Microbial susceptibility across India

Technical Expertise

  • Serotyping, Phenotyping
  • Phase-contrast microscopy
  • Viability assays
  • Microbial based biochemical assays

Formulation Development

  • NDDS, Nanotechnology based formulation
  • Polymer conjugates (DPPC)
  • Pilot and scale up facilitation
  • IV to oral formulations

Technical Expertise

  • Sustained release formulations
  • Targeted deliveries to anti-infectives, oncology

Pre-clinical & Toxicological Research

Technical Expertise

  • Anti-infective
  • Oncology
  • Pain and inflammation
  • Wound care
  • Diabetes
  • Hyperlipidaemia
  • CNS disorders
  • GIT disorders


  • In-vivo pharmacology
  • Toxicity studies
  • Drug metabolism and PK
  • Animal model validation
  • Histopathology studies
  • Safety pharmacology
  • Exposure/Response studies

Clinical Research & PMS

  • PHASE 1,2,3 Trials
  • PMS studies
  • Investigator initiated trials
  • Monitoring of trials

Technical Expertise

  • Anti-infective
  • Oncology
  • Pain and inflammation
  • Wound care and Diabetes

Drug Regulatory Affairs

  • CTD filings, USFDA, EMEA, TGA, MCC, India and Rest of the world
  • Change Control
  • EVMPD Compliance
  • Tracking and reporting
  • Technical Expertise
  • M2, M3, M4, M5 component of drug dossiers filing
  • eCTD submission compliance
  • IND, Pre-IND meets meetings

Intellectual Property Consultation

  • Patentability & Prior Art Search
  • Drafting complete application
  • Filings in India & PCT member countries
  • Patent Grant & Maintenance
  • Trademark searching, filing, prosecution, opposition & maintenance
  • Copyright filing & maintenance

Satisfied Clients


Dr. Manu Chaudhary

JMD & Director Research


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