Auriga Research's Bangalore facility provides NABL-accredited pharmaceutical testing services for South India's pharma manufacturers. Covering assay and impurity profiling, dissolution studies, stability testing, microbiological analysis, and analytical method development from our Yeshwanthpur laboratory.
GMP-compliant pharmaceutical quality control and analytical services for APIs, formulations, and packaging materials.
HPLC and GC-based assay determination, related substances, degradation impurities, and residual solvents per ICH guidelines.
USP apparatus I-IV dissolution testing, dissolution profiling, and in-vitro release studies for solid and semi-solid dosage forms.
ICH-compliant accelerated (40C/75% RH), intermediate, and long-term stability studies with photostability testing.
Microbial limit testing, sterility testing, bacterial endotoxin testing, and environmental monitoring per USP/IP.
API identity, purity, and quality testing. Excipient testing per pharmacopoeial monographs (IP, USP, EP, BP).
Analytical method development and ICH Q2(R1) validation for novel formulations and combination products.
Bangalore and the wider Karnataka region host a substantial pharma manufacturing base, including API producers, formulation units, and biotech companies. Our Yeshwanthpur laboratory provides local testing support that eliminates the need to ship samples to Delhi or Mumbai for routine QC and compliance testing.
The facility handles the full range of pharmacopoeial testing per IP, USP, EP, and BP monographs — from raw material identification and assay to finished product quality testing. Advanced instrumentation including HPLC, GC, and ion chromatography systems enables comprehensive analytical coverage.
For the complete scope of pharmaceutical testing services, visit our national pharmaceutical testing service page. For accreditation details, see our NABL accreditation page.
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NABL-accredited pharma QC and analytical services. Serving South India from Yeshwanthpur.
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