Baddi Lab · NABL Accredited · ISO 9001:2015 · COS 23 · Form-37 Drug

Pharmaceutical Testing in Baddi | NABL Accredited Lab | Auriga Research

On-site QC for the Baddi-Nalagarh-Barotiwala pharma cluster.

The Auriga Research Baddi laboratory provides NABL-accredited pharmaceutical testing under ISO/IEC 17025:2017 (Certificate TC-5350) directly inside the Baddi-Nalagarh-Barotiwala manufacturing zone. The facility covers QC release, raw material testing, dissolution, stability, and microbiological testing for finished formulations, APIs, excipients, and packaging materials.

Get a Quote for Baddi Lab Testing Call +91- 7428116100

Baddi Lab Address

Dev Chaudhary Complex, Bagbania, Baddi-Nalagarh Road, Solan 174102, HP

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

Phone: +91 7428116100

Email: info@aurigaresearch.com

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What the Baddi Lab Tests

Five core pharmaceutical testing categories confirmed in the Baddi NABL scope.

QC Release Testing

Finished formulation batch release testing against IP, USP, BP, and EP monographs for the Baddi-Nalagarh-Barotiwala manufacturing zone.

Raw Material Testing

API identity, purity, and pharmacopoeial conformity testing. Excipient testing for incoming materials per applicable monographs.

Dissolution Testing

USP apparatus dissolution testing and dissolution profiling for solid and semi-solid dosage forms under NABL-accredited conditions.

Stability Studies

ICH-aligned accelerated, intermediate, and long-term stability studies with controlled chambers and documented protocols.

Microbiological Testing

Microbial limits, sterility testing, bacterial endotoxin testing, and pharmaceutical microbiology per IP and USP.

Key Parameters Tested

The most-requested analytical parameters at the Baddi pharmaceutical testing lab.

Assay & Potency

Quantitative assay of active pharmaceutical ingredients by HPLC, UV, and titrimetric methods against pharmacopoeial limits.

Dissolution & Disintegration

USP apparatus dissolution and disintegration testing per monograph, including profiling and comparative studies.

Microbial Limits & Sterility

Total aerobic microbial count, total yeast and mould count, absence of specified pathogens, and sterility testing.

Water Activity

Water activity (aw) determination for moisture-sensitive solid dosage forms and shelf-life prediction.

Particle Size

Particle size distribution analysis for solid dosage forms, suspensions, and inhalation products.

Why Use the Baddi Lab

Three reasons pharmaceutical manufacturers in the Baddi-Nalagarh-Barotiwala zone choose the Auriga Baddi lab.

Proximity to the Baddi-Nalagarh-Barotiwala Pharma Cluster

The lab sits inside one of India's most concentrated pharmaceutical manufacturing zones, with rapid same-day or next-day sample receipt from local units.

On-Site QC Reduces Sample Transit Time

Local testing removes the courier transit window to Delhi or Chandigarh, accelerating batch release and stability programmes for Baddi-zone manufacturers.

NABL Reports Accepted by CDSCO and Export Buyers

NABL-accredited reports are accepted by CDSCO, the Himachal Pradesh State Drug Controller, export agencies, and international regulatory authorities and buyers.

How It Works

Four steps from initial enquiry to digital report. Standard TAT 5 to 7 working days. Express testing available.

01

Contact the SPOC

Call your single point of contact at +91 74281 16100 to confirm the test scope, applicable standard, and receive sample submission details.

02

Submit Samples

Drop samples at the Baddi lab address or send by courier with pre-approval. Each sample is bar coded on receipt and registered in YLIMS.

03

Testing Under NABL

Testing is conducted under NABL-accredited conditions with in-process quality checks at each step against the applicable pharmacopoeial standard.

04

Report via YLIMS

The digital report is issued and accessible via YLIMS. Standard TAT is 5 to 7 working days. Express testing options are available for time-critical batches.

Accreditations and Approvals

Credentials held at the Baddi facility supporting pharmaceutical testing.

NABL logo
NABL

ISO/IEC 17025:2017, Certificate TC-5350

ISO 9001:2015 logo
ISO 9001:2015

Quality management system certification

COS 23
COS 23

Cosmetics conformity testing scheme

Form-37 Drug
Form-37 Drug

Pharmaceutical drug testing licence

Get a Quote for Baddi Lab Testing

NABL TC-5350 accredited pharmaceutical testing at the Baddi facility. Standard TAT 5 to 7 working days. Express options available.

+91-7428116100 Get a Quote for Baddi Lab Testing

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