NABL Accredited

Pharmaceutical Testing Laboratory in Gurugram | NABL Accredited

Auriga Research's Gurugram facility provides NABL-accredited pharmaceutical testing services for the NCR pharma corridor. Specialising in particle size analysis alongside standard QC testing — assay, dissolution, stability, and microbiological analysis — from our Udyog Vihar laboratory.

Request a Quote Call +91- 7428116100

Lab Address

Plot No. 235, Udyog Vihar Phase IV, Gurugram 122016

Hours: Mon-Sat, 9AM-5PM IST

Phone: +91 7428116100

Email: info@aurigaresearch.com

NABL

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Pharmaceutical Testing Services

GMP-compliant pharmaceutical quality control with specialised particle size analysis capability for the NCR pharma corridor.

Assay & Impurity Profiling

HPLC and GC-based assay determination, related substances, degradation impurities, and residual solvents per ICH guidelines.

Dissolution Studies

USP apparatus I-IV dissolution testing, dissolution profiling, and in-vitro release studies for solid and semi-solid dosage forms.

Stability Testing

ICH-compliant accelerated (40°C/75% RH), intermediate, and long-term stability studies with photostability testing.

Particle Size Analysis

Laser diffraction-based particle size distribution analysis for APIs, excipients, and finished dosage forms.

Raw Material Testing

API identity, purity, and quality testing. Excipient testing per pharmacopoeial monographs (IP, USP, EP, BP).

Microbiological Testing

Microbial limit testing, sterility testing, bacterial endotoxin testing, and environmental monitoring per USP/IP.

Pharmaceutical Testing in Gurugram

Gurugram and the wider Manesar-IMT industrial belt host a growing number of pharmaceutical manufacturers, CROs, and biotech companies. The Gurugram facility provides local testing support for the NCR pharma corridor, reducing sample transit time and enabling faster batch release and regulatory submissions.

A key differentiator of the Gurugram laboratory is its specialised particle size analysis capability using advanced laser diffraction technology — essential for API characterisation, formulation development, and in-process quality control. The facility also handles the full range of pharmacopoeial testing per IP, USP, EP, and BP monographs for routine batch release and stability studies.

For the complete scope of pharmaceutical testing services, visit our national pharmaceutical testing service page. For accreditation details, see our NABL accreditation page.