Nutraceuticals and dietary supplements require precise testing for identity, potency, and purity. Auriga Research tests vitamins, minerals, probiotics, protein supplements, and botanical extracts against FSSAI, USP, and international pharmacopeial standards. Our NABL-accredited results support both Indian regulatory filings and export documentation.
Vitamin assay (A, B-complex, C, D, E, K), mineral content, amino acid profiling, and active compound quantification by HPLC and ICP-OES.
Heavy metals, pesticide residues, mycotoxins, melamine, and solvent residues. Testing per FSSAI limits and USP <561> / <565> requirements.
Total plate count, yeast and mold, coliforms, E. coli, Salmonella, and Staphylococcus aureus. Probiotic viability counts for probiotic supplements.
Accelerated and real-time stability for shelf life determination. Potency retention, moisture uptake, and organoleptic changes tracked at defined intervals.
In India, nutraceuticals are regulated under FSSAI (Food Safety and Standards Act) with specific provisions under the Health Supplements, Nutraceuticals, and Similar Products Regulations. Every product requires testing for identity, purity, and safety before it can be sold.
For products targeting the US market, we test per USP dietary supplement monographs and 21 CFR Part 111 (cGMP) requirements. Our USFDA registration ensures reports are accepted for US regulatory purposes.
Share your product formulation and target market. We will recommend the right testing panel and provide a quote within 24 hours.
Download a practical testing guide tailored to your industry — checklists, parameters, and regulatory tips in one place.
Get Free Guide Request a Quote InsteadNo thanks, I'll keep browsing