Bangalore Lab · NABL TC-5496 · WHO Prequalified · USFDA Inspected

Pharmaceutical Testing Laboratory in Bangalore | NABL Accredited | WHO Prequalified

The Bangalore Pharmaceutical Testing Laboratory at Yeshwanthpur provides NABL-accredited pharmaceutical testing under ISO/IEC 17025:2017 (Certificate TC-5496) for South India pharmaceutical and biotech manufacturers. The 13-entry pharmaceutical scope under NABL covers stability, assay, dissolution, and microbiological testing, supported by WHO Prequalified and US FDA-inspected analytical capability.

Bangalore Lab Address

136, 6th Cross Rd, 2nd Stage, Yeshwanthpur, Bengaluru 560022

NABL Certificate: NABL TC-5496

Validity: Valid until March 2026 (renewal in progress)

Phone: +91 74281 16100

Email: [email protected]

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What the Bangalore Lab Tests for Pharmaceuticals

Six pharmaceutical testing categories confirmed in the Bangalore NABL pharmaceutical scope (TC-5496, 13 entries).

Stability Studies

Real-time and accelerated stability studies under ICH-aligned conditions for finished pharmaceutical formulations.

Assay Determination

HPLC and titrimetric assay of active pharmaceutical ingredients in finished dosage forms against pharmacopoeial monographs.

Dissolution Testing

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

Microbiological Testing

Microbial limits, total plate count, yeast and mould, and pathogen testing for non-sterile pharmaceutical products per USP and IP.

Raw Material Testing

Identity, purity, and pharmacopoeial conformity testing for incoming APIs and excipients within the accredited scope.

Finished Product Release

Batch release testing for finished pharmaceutical formulations against established specifications and pharmacopoeial limits.

Scope note: For nitrosamine impurity testing (ICH M7), endotoxin testing (LAL / rFC), advanced impurity profiling, and method development and validation, route clients to the Delhi (NABL TC-7375) or Manesar (NABL TC-15532) facilities.

Why Use the Bangalore Lab for Pharmaceutical Testing

Three reasons pharmaceutical and biotech companies across Karnataka and South India choose the Bangalore lab.

WHO Prequalified

Reports accepted for international regulatory submissions, WHO PQ tender packages, UN agency procurement, and Global Fund workflows.

USFDA Inspected

US FDA-inspected pharmaceutical testing facility. Reports accepted by US market buyers, contract manufacturers, and US importers.

Karnataka & South India Presence

Ideal for pharmaceutical companies in Karnataka and South India requiring locally issued, internationally accepted analytical certificates.

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 pharmacopoeial standard, and sample submission details.

02

Submit Samples at Yeshwanthpur

Drop the sample at the Yeshwanthpur address or send by pre-approved courier. Each sample is bar coded on receipt and registered in YLIMS.

03

Testing Under NABL Conditions

Testing is conducted under NABL-accredited conditions (TC-5496) with in-process QA checks 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 available.

Accreditations and Approvals

Three credentials held at the Bangalore facility supporting pharmaceutical testing.

NABL TC-5496 logo
NABL TC-5496

ISO/IEC 17025:2017, Valid Mar 2026 (renewal in progress)

WHO Prequalified logo
WHO Prequalified

WHO PQ recognition for analytical testing scope

USFDA Inspected logo
USFDA Inspected

US FDA inspected pharmaceutical testing facility

Get a Quote for Bangalore Pharma Testing

NABL TC-5496 accredited pharmaceutical testing. WHO Prequalified and US FDA-inspected facility. Standard TAT 5 to 7 working days. Express options available.

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