Consumer demand for Ayurveda and herbal medicines keeps growing — and so do concerns about safety and quality. Ayurvedic and herbal product testing is mandatory in today's market because natural ingredients can be contaminated by microbes, heavy metals or pesticide residues.
Ensure herbs are authentic and free from adulterants — checking botanical identity and active compounds.
ICP-MS and AAS quantify toxic metals and pesticide residues, mandatory under AYUSH and export standards.
Testing for bacteria (E. coli, Salmonella), moulds and yeasts.
Detailed profiling of bioactive compounds — alkaloids, flavonoids, glycosides.
Determine how long your product remains effective and safe — essential for labelling and export.
The full regulatory guide — stability studies, Form 48/49, and the 2026 shelf-life rule change.
Explore e-Aushadhi Testing Guide →Share your product and use-case — we suggest the right test panel.
Clear pricing with turnaround time and sample requirements.
Pan-India sample collection with proper chain-of-custody.
Compliant, audit-ready PDFs with expert interpretation.
Meets ISO/IEC 17025 standards, recognised by BIS and FSSAI.
Protocols align with AYUSH, FSSAI and WHO pharmacopoeial standards.
HPLC, GC-MS/MS, ICP-MS and AAS for precise analysis.
Specialists in herbal identification, raw material verification and finished product testing.
Samples collected and reports delivered nationwide.
"As a manufacturer of Ayurvedic formulations, we needed a trusted partner to validate our raw herbs and finished capsules. The AYUSH-accredited team provided detailed reports on identity, purity and heavy-metal levels, helping us launch our products with confidence."
Yes. Regulatory bodies require testing of raw materials and finished products for identity, authenticity, heavy metals, toxins and microbial contamination. Without proof of testing, products cannot be legally marketed or exported.
Botanical identity, active ingredients, heavy metals, pesticide residues, microbial contamination and stability.
Every batch of raw materials and each lot of finished product — shelf-life studies are required for new formulations and periodically thereafter.
Yes — our test reports meet national and international standards, suitable for export documentation.
Yes — our scientists guide active ingredient concentrations and help optimise formulations for efficacy and compliance.
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