Services
Every service below can be engaged on its own or as part of a broader export-readiness strategy across India, the GCC, the EU, the US, and Australia. Enquire through the portal and we'll scope it against your specific formulation and timeline.
Audit-safe technical dossiers built to the standard of the market you're entering — safety data compilation, evidence packages, and full submission stacks structured to hold up under a regulator's second look, not just the first pass.
FSSAI product approvals, licensing, and category classification under nutraceutical and health supplement regulations — new licence applications, product approval filings, and renewals — plus ongoing advisory as rules shift. We build the file to withstand scrutiny at every renewal cycle, not just clear the first review.
Formulation and reformulation guidance combined with toxicological safety review — keeping a product's efficacy intact while meeting the permissible-ingredient list, dosage limits, exposure thresholds, and claim restrictions of each target market.
Label-ready submissions and packaging review calibrated to India (FSSAI), GCC (MoHAP), EU (Novel Food and health claims rules), US (FDA / DSHEA), and Australia (TGA) requirements at the same time — built once for every market you're entering, not re-done market by market after a rejection.
Sourcing and raw-material risk review grounded in ground-level field research, not desk research alone — GACP compliance, aflatoxin and contamination risk, verification against NABL-accredited labs, and the batch-clubbing issues that quietly derail export consignments at the port.
An independent review of a brand or ingredient's regulatory standing — licence validity, open queries, and pending submissions — ahead of an investment, distribution partnership, or acquisition decision.
Describe your product and stage in a short enquiry — we'll tell you plainly what applies and what doesn't, before any fee is discussed.
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Arvena