NABL Accredited · AYUSH Compliant

Herbal & AYUSH Product Testing Laboratory India | NABL Accredited

Auriga Research is a NABL-accredited testing laboratory for herbal, Ayurvedic, Siddha, Unani, and Homeopathy products. We test for heavy metals, pesticide residues, microbial contamination, aflatoxins, and undeclared synthetic drugs. Our stability testing of herbal drugs supports shelf-life claims and AYUSH product registration.

Reports in 7-10 working days | Stability studies from 28 days

Request Testing Call +91-7428116100

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Accreditations & Approvals

NABL

CDSCO

FSSAI

WHO

BIS

USFDA

AYUSH

APEDA

ISO

EIC

NABL

CDSCO

FSSAI

WHO

BIS

USFDA

AYUSH

APEDA

ISO

EIC

The Challenge

Herbal and AYUSH manufacturers face tightening regulations on heavy metal limits, pesticide residues, and undeclared drug adulteration. The Ministry of AYUSH and CDSCO require accredited test data for product licensing. Without reliable testing, products risk rejection, recalls, and reputational damage.

Our Solution

Auriga Research provides NABL-accredited herbal testing with pharmacopoeial-grade methods for heavy metals, pesticides, microbiology, and steroid detection. Our stability testing programme for herbal drugs generates the shelf-life data required for AYUSH registration, ensuring your products meet every regulatory checkpoint.

Herbal & AYUSH Testing Services

End-to-end testing for herbal raw materials, botanical extracts, and finished AYUSH products — from identity to stability.

Heavy Metals Testing

Lead, mercury, arsenic, and cadmium quantification by ICP-MS as per API, WHO, and USP limits for herbal products.

Pesticide Residue Analysis

Multi-residue screening for 200+ pesticides in botanical raw materials and finished herbal products by GC-MS/LC-MS/MS.

Microbial Limits Testing

Total aerobic count, yeast and mould, E. coli, Salmonella, and Staphylococcus aureus testing per pharmacopoeial methods.

Aflatoxin Testing

Aflatoxins B1, B2, G1, G2, and total aflatoxin quantification by HPLC and LC-MS/MS for raw herbs and finished products.

Stability Testing of Herbal Drugs

Accelerated and real-time stability studies under ICH Zone IV conditions for shelf-life determination and AYUSH registration.

Marker Compound Analysis

HPTLC and HPLC-based identification and quantification of active marker compounds for identity and potency verification.

Phytochemical Screening

Qualitative and quantitative screening for alkaloids, flavonoids, tannins, saponins, and other phytochemical classes.

Residual Solvent Testing

GC-based residual solvent analysis for herbal extracts as per ICH Q3C and pharmacopoeial requirements.

Testing for Steroids and Undeclared Drugs

Adulteration of herbal and Ayurvedic products with undeclared synthetic drugs is a serious regulatory and safety concern. Auriga Research operates a dedicated LC-MS/MS screening programme to detect corticosteroids (dexamethasone, betamethasone, prednisolone), NSAIDs (diclofenac, piroxicam), PDE5 inhibitors (sildenafil, tadalafil), and other commonly adulterated synthetic compounds in herbal formulations.

This testing is essential for manufacturers facing regulatory audits, brands protecting consumer safety, and exporters meeting destination-country requirements. Our screening methods are validated against USP and WHO guidelines, and results are issued under NABL accreditation.

Need steroid or drug adulteration testing for your herbal product? Submit a sample for NABL-accredited LC-MS/MS analysis.

Submit a Sample for Testing Learn More: Steroids in Herbal Medicines

Why Choose Auriga for Herbal & AYUSH Testing

NABL accreditation ensures test reports are accepted by Ministry of AYUSH, CDSCO, and state licensing authorities.

Dedicated steroid and undeclared drug screening by LC-MS/MS — protecting your brand from adulteration risks.

Complete pharmacopoeial testing — API, UPI, SPI, IP, USP — for identity, purity, and potency of herbal ingredients.

Accreditation and Compliance

Auriga Research holds NABL accreditation under ISO/IEC 17025:2017 for herbal and AYUSH product testing. Our scope covers heavy metals by ICP-MS, pesticide residues by GC-MS/LC-MS/MS, microbiological testing, aflatoxin analysis, and stability studies under ICH-aligned conditions.

Test reports are accepted by the Ministry of AYUSH for product licensing, CDSCO for drug registration, state AYUSH licensing authorities, and export regulatory bodies. Our methods align with Ayurvedic Pharmacopoeia of India (API), WHO guidelines for herbal medicines, and USP monographs for botanical products.

Proven Track Record

An Ayurvedic manufacturer required urgent steroid screening after a regulatory query flagged one of their formulations. Auriga Research completed LC-MS/MS screening for 30+ synthetic compounds within 5 working days, confirmed the product was free of undeclared drugs, and issued a NABL-accredited certificate of analysis. The report cleared the regulatory query and the product remained on the market without disruption.

Get Your Herbal Products Tested

NABL-accredited herbal and AYUSH testing. Heavy metals, pesticides, steroids, stability studies, and full pharmacopoeial analysis.

+91-7428116100 Request Testing

Frequently Asked Questions

What testing is required for AYUSH product registration in India?

AYUSH product registration requires testing for heavy metals (lead, mercury, arsenic, cadmium), microbial limits, pesticide residues, aflatoxins, and product-specific identity and assay tests. Products must comply with Ayurvedic Pharmacopoeia of India (API), Unani Pharmacopoeia of India (UPI), or Siddha Pharmacopoeia of India (SPI) as applicable. Auriga Research provides NABL-accredited testing covering all parameters required by the Ministry of AYUSH.

Can you test herbal products for undeclared steroids and drugs?

Yes. We operate a dedicated screening programme for undeclared synthetic drugs and steroids in herbal and Ayurvedic products. Using LC-MS/MS methods, we screen for corticosteroids (dexamethasone, prednisolone), NSAIDs, PDE5 inhibitors, and other commonly adulterated synthetic compounds. This testing is critical for manufacturers facing regulatory scrutiny and for brands protecting their reputation.

How long does stability testing of herbal drugs take?

Accelerated stability testing for herbal drugs runs for 6 months under ICH-aligned conditions (40 degrees C, 75% RH). Real-time studies run for 12-36 months depending on claimed shelf life. Auriga Research provides interim reports at each time point for regulatory submission. Zone IV climatic conditions specific to India are used as the default for domestic market products.

Are your herbal testing reports accepted by the Ministry of AYUSH?

Yes. Auriga Research holds NABL accreditation under ISO/IEC 17025:2017 for herbal and AYUSH product testing parameters. Our certificates of analysis are accepted by the Ministry of AYUSH, state AYUSH licensing authorities, and CDSCO for Ayurveda, Siddha, Unani, and Homeopathy product registrations.

What is the cost of herbal product testing in India?

Costs vary by test panel and product type. Heavy metals analysis starts from approximately Rs 4,000-8,000 per sample. Microbial limits testing ranges from Rs 3,000-6,000. Steroid screening panels start from Rs 8,000-15,000. Complete AYUSH registration panels are quoted based on your specific product category. Contact us for a detailed quotation.