About the lab

An independent analytical laboratory for pharmaceutical testing

The Analytical Lab operates from Chhatral, Gujarat, serving formulation and API manufacturers across development and commercial supply. We take on the analytical work that sits between a product and its release — building the method, proving it, and running it batch after batch.

Every result we issue is traceable to a written method, a calibrated instrument and a second review. That traceability is what makes data usable in a submission, and it is the reason clients hand us work they cannot afford to repeat.

Quality control testing laboratory with high precision analytical equipment and dual analyst verification

Chhatral, Gujarat

GIDC Phase 2 — accessible from Ahmedabad and Gandhinagar.

Independent lab

No manufacturing interest in the products we test.

NABL accreditation in progress.

What we do

Three kinds of work, one quality system

Whether a product is in development or in production, it runs through the same documented methods, the same instrument qualification and the same review before a report leaves the building.

Method development & validation

Chromatographic methods built for the product in front of us, challenged by forced degradation, and validated with a protocol and report you can file.

Routine & release testing

Assay, related substances, residual solvents, dissolution and the full set of physical tests — reported as a COA with the supporting data behind it.

Stability studies

ICH condition studies run to a written protocol, with interval testing, trend data and a study report at the end of the programme.

How we work

Four commitments we hold on every project

These are not aspirations. They are the checks a sample passes through between arriving at goods-in and appearing on a signed report.

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Nothing runs without a written method

Every test follows an approved STP or pharmacopeial monograph — never an undocumented in-house shortcut.

Every number is reviewed by a second analyst

Calculations and chromatograms are checked against acceptance criteria before the report is released.

Raw data stays with the report

Chromatograms, weighings and standard details are retained and supplied on request for audit or filing.

Your product stays confidential

Samples, methods and results are treated as your property. We sign NDAs before samples ship.

Capability

Techniques and standards

Our analytical work is chromatography-led, supported by the wet chemistry and physical testing that a complete specification needs.

HPLC Assay, related substances, dissolution, content uniformity

GC / GC-HS Residual solvents, volatile impurities

Dissolution Method development, profile comparison, disintegration

Wet chemistry Titration, water content, LOD, pH, sulphated ash

Standards and guidelines

We work to the pharmacopeia your specification names, and validate to ICH expectations.

IP USP BP EP ICH Q1A ICH Q2

Documentation we issue

Certificates of Analysis

Validation protocols and reports

SOPs and standard test procedures

Stability study protocols and reports

Working with us

What it is like to send us work

You talk to the analyst

Technical questions go straight to the person running your samples — not through an account manager.

Scope agreed in writing first

Tests, specification, turnaround and cost are confirmed before a sample is opened. No surprise line items.

Support after the report

Queries on results, repeat testing and method transfer to your own lab are part of the engagement.