- Method development and validation for Nitrosamine analysis
- Genotoxic Impurities- Method development and validations for Genotoxic Impurities
- Elemental Impurities study as per ICH Q3D guidelines
- Method development and validation as per ICH Q2 and USP 1225
- Method Verification as per USP 1226
- Polymorphic Method Development (Validation and Batch Analysis using XRD, DSC and TGA)
- Analytical Method Development and Validation for Assay, Related substances, Residual Solvents, Dissolution and Content uniformity.
Our Process
The Management of MART Specialities Lab, LLP aim for continual improvement in Quality services provided to their customers by establishing compliance with Management System as per ISO/IEC 17025:2017.
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1
Sample Registration
Our sample registration process secures the confidentiality of the customer and establishes traceability to the results.
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2
Sample analysis
All our instruments are with 21CFR part 11 compliant software. This ensures that the data generated is in its purest form.
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3
Review of analysis
A two-step data review procedure that ensures accuracy of the data generated.
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4
Release of Certificate of Analysis
Release of COA with authentic information that makes movement of your product easier in the market.