NABL accredited laboratory, TC-5843
· Jaipur, Rajasthan

7 to 10 working days

Standard turnaround from sample receipt

NABL TC-5843

Accredited to ISO/IEC 17025:2017

HPTLC with documentation system

Primary technique on this service

14,000 sq. ft.

Integrated laboratory in Jaipur

In plain language

This service applies the Ayurvedic Pharmacopoeia of India to raw herbs and finished formulations: identity, ash values and extractives that confirm what the material is, then heavy metals, pesticide residues, aflatoxins and microbial limits that confirm it is safe. Marker compound assay by HPLC or HPTLC quantifies the active constituent.

When to use this test

Rule 158B testing for an AYUSH manufacturing licence

Exporting Ayurvedic or herbal products to the EU, US or Gulf

Accepting crude drug consignments of unknown origin

Applying for the AYUSH premium mark or a buyer audit

Parameters

What we test on this service

Panels are built from the list below. Tell us the market and the specification and we select the parameters it calls for rather than selling you the whole sheet.

01

Identification, description and organoleptic checks

02

Loss on drying, total ash, acid insoluble ash, extractives

03

Heavy metals: lead, cadmium, arsenic, mercury

04

Pesticide residues and aflatoxins

05

Microbial limits and specific pathogens

06

Marker compound assay by HPLC and HPTLC


Method

How the analysis runs

Instrumentation and controls

Every batch runs with the controls its method requires, on calibrated equipment, and a second analyst reviews the data before the report is released.

Techniques HPTLC with documentation system, HPLC with DAD
Supporting equipment ICP-MS and mercury analyser, GC-MS/MS for residues
Accredited scope NABL TC-5843
Standard turnaround 7 to 10 working days
Reporting Result, limit, method and uncertainty

Standards and methods

Results are reported against the method below, or against your buyer's specification where you send one with the sample.

Ayurvedic Pharmacopoeia of India, all parts Drugs and Cosmetics Act, Schedule T and Rule 158B AYUSH premium mark testing requirements WHO guidelines on quality of herbal medicines

Ask for the full NABL scope document if you need to confirm accredited coverage before sending the sample.

Not sure which parameters your buyer wants?

Send us the specification. We will tell you what to test and what it costs, at no charge.

Request a quote
Regulatory context

The approvals this work is issued under

Our AYUSH and herbal capability came with the CEG Test House acquisition and is accredited under NABL TC-5843, covering Rule 158B testing and the export panels overseas buyers ask for.

Accreditation
NABL ISO/IEC 17025, TC-5843

Before you send it
Sample quantity and packing

100 g of powder or churna, 100 tablets or capsules, 250 ml of liquid asava or arishta, with the formulation composition sheet.

Turnaround time

7 to 10 working days for a full pharmacopoeial panel including residues.

Who this is for

Ayurvedic and herbal manufacturers


AYUSH exporters, including to the EU and US


Contract manufacturers and traders in raw herbs


Licensing and regulatory consultants

Send a sample

Fill in the Test Request Form, pack the sample as described above and courier it to the Jaipur laboratory. Call us first if the sample is perishable.

Get the TRF

Related queries

Questions we get asked

Do you test raw herbs as well as finished products?

Yes. Raw drug authentication, ash values, extractives and contamination screening on the crude drug, and full pharmacopoeial testing on the finished formulation.

Which panel does an AYUSH export need?

Usually heavy metals, pesticide residues, aflatoxins and microbial limits with the pharmacopoeial identity work. We confirm against your destination market.

Can you authenticate a crude drug with no label?

Macroscopic and microscopic examination with HPTLC fingerprinting will usually confirm or rule out the claimed species.

Why do heavy metals appear in a clean formulation?

Almost always from the raw herb or the soil it grew in. Screening incoming material is cheaper than reworking a finished batch.

Do bhasma and rasa preparations need a different panel?

Yes. Metal-based preparations are tested against their own pharmacopoeial specifications rather than the general heavy metal limits.


Request a quote

Tell us what you need tested


Send the product, the market it ships to and the standard you are being held to. Our technical team replies with the parameter list, the sample quantity we need and a firm turnaround. Quotes usually go out the same working day.

+91-9950229764 / +91-9634063932

Sample receipt: Monday to Saturday, 9:30 am to 6:00 pm

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