Pharmaceutical Testing Services | Contract Testing Laboratory India

Auriga Research provides comprehensive contract testing for pharmaceutical manufacturers, CROs, and API suppliers. From raw material identity to finished product release testing, our NABL-accredited and USFDA-registered laboratories deliver pharmacopeial-grade results on time.

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What We Test for Pharma

API and Excipient Testing

Identity, assay, related substances, residual solvents, heavy metals, and water content per IP, BP, USP, and EP monographs.

Finished Product Testing

Content uniformity, dissolution, disintegration, hardness, friability, and assay for tablets, capsules, injectables, and topicals.

Stability Studies

ICH Q1A accelerated and long-term stability. Photostability per Q1B. Walk-in stability chambers with 24/7 monitoring and alarm systems.

Impurity Profiling

Genotoxic impurities (ICH M7), elemental impurities (ICH Q3D), nitrosamine screening, and degradation product identification.

Why Pharma Companies Choose Auriga

1

USFDA Registered, NABL Accredited

Reports accepted for ANDA, NDA, and CDSCO filings. No re-testing at the reviewer's end.

2

Multi-Compendial Capability

We test against IP, BP, USP, EP, and JP monographs. One lab for all your market requirements.

3

7-10 Day Standard Turnaround

Express options available for urgent batch release. Real-time status tracking for every sample.

Need Pharmaceutical Testing?

Share your product details and testing requirements. Our pharma team will provide a detailed quote within 24 hours.

+91-7428116100 Request a Quote

Related Services

Pharmaceutical Testing

Complete list of pharmaceutical tests and methods.

Testing Scope

Full capabilities across all testing categories.

Testing Charges

Indicative pricing for pharmaceutical testing.

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