NABL Accredited

Pharmaceutical Testing Laboratory in Baddi | NABL Accredited

Auriga Research operates Himachal Pradesh's largest NABL-accredited pharmaceutical testing laboratory in the Baddi manufacturing zone. Strategically located to serve 700+ pharma manufacturing units, the facility provides on-site QC testing that eliminates the need to ship samples to Delhi or Chandigarh.

Request a Quote Call +91- 7428116100

Lab Address

Plot No. 29, Sector 6A, EPIP, Baddi, Himachal Pradesh 173205

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

Phone: +91 7428116100

Email: info@aurigaresearch.com

NABL

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Pharmaceutical Testing Services

Full-service pharmaceutical QC testing for APIs, formulations, and packaging materials — right in the Baddi pharma zone.

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.

Microbiological Testing

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

Raw Material Testing

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

Packaging Material Testing

Container closure integrity, extractables and leachables, moisture vapour transmission, and compatibility studies.

Pharmaceutical Testing in Baddi

Baddi-Barotiwala-Nalagarh is one of India's most prominent pharmaceutical manufacturing zones, with over 700 manufacturing units producing APIs and finished dosage forms. The cluster's rapid growth has created strong demand for local NABL-accredited testing infrastructure that can support batch release, stability studies, and regulatory compliance without transit delays.

Our Baddi facility handles the full range of pharmacopoeial testing per IP, USP, EP, and BP monographs. Proximity to manufacturing units enables same-day sample collection and faster turnaround — critical for production schedules and regulatory timelines. The laboratory supports both routine QC and complex analytical work including stability studies and packaging material compatibility testing.

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