Comparator Studies
VIMTA offers analytical support to evaluate new drug products in development with marketed drug products of the same therapeutic class. The comparator studies also provide reference point for clinical trials by helping in analysis of relative bioequivalence, efficacy and safety.
Our services include:
- Assay
- Dissolution
- Impurity profiling
- Stability studies
Other Services
- Analytical Services for Preclinical
- API Analysis
- Cleaning Method Validations
- Contraceptives Testing
- Disintegration Studies
- Dissolution Studies
- ELISA Assays
- Extractables & Leachables
- Formulation Optimization Studies
- Ink & Gum Migration studies
- Glass Delamination Studies
- GLP Tox Release Testing, DS & Impurities
- Gluten Free Claim Testing
- Impurity Analysis
- IND & NDA Submission Support
- Inhalation Product Analysis & Testing
- Biowaiver Studies
- Method Development & Validation, and Transfers
- Microbiological Testing and Evaluation
- Naso-gastric In Vitro Studies
- Non Biologics Complex Drugs (NBCD) Testing Services
- OVI / Residual Solvent Studies
- Packaging Material Testing
- Pharmacopoeial Monograph Testing
- Pre-shipment Inspection & Testing Services
- Product Defect Investigations
- Purposeful Degradation Studies
- QC Testing for Batch Release
- Raw Material & Excipient Qualification
- Reference Standard Characterization
- Residual Genotoxic Impurity Studies
- Solid State Characterization & Polymorph Quantification
- Stability and Release Testing
- Elemental Analysis
- Water Quality Analysis
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