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
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.
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
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.
Identification, description and organoleptic checks
Loss on drying, total ash, acid insoluble ash, extractives
Heavy metals: lead, cadmium, arsenic, mercury
Pesticide residues and aflatoxins
Microbial limits and specific pathogens
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.
Standards and methods
Results are reported against the method below, or against your buyer's specification where you send one with the sample.
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.
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.
Before you send it
100 g of powder or churna, 100 tablets or capsules, 250 ml of liquid asava or arishta, with the formulation composition sheet.
7 to 10 working days for a full pharmacopoeial panel including residues.
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 TRFRelated 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