Health intelligence & regulatory consultancy

Regulatory and formulation-safety consulting for nutraceutical brands going cross-border

Regulatory and formulation expertise, applied for the first time under Arvena's own name — FSSAI · GCC · EU · US.

Arvena Sciences prepares audit-safe scientific dossiers, formula safety assessments, and label-ready submissions for nutraceutical and functional food brands moving across India, the GCC, the EU, and the United States — turning regulatory complexity into a competitive advantage instead of a bottleneck.

At a glance
Focus areas
Nutraceuticals · Functional foods · Supplements
Jurisdictions
India (FSSAI) · US (FDA) · EU (EFSA) · UAE/GCC (MoHAP) · Australia (TGA)
Engagement model
Project or retainer
Client portal
Secure, always-on access
Typical response time
Within 1 business day
Nutraceutical products across export markets

Where we help

We help companies build categories, enter markets, avoid costly mistakes and create defensible business. Six areas where regulatory missteps cost the most time, money, and shelf life — and where we spend most of our working hours.

SD

Scientific dossiers

Audit-safe technical dossiers built to the standard of the market you're entering — safety data compilation, evidence packages, and full submission stacks that hold up under a regulator's second look.

RA

Regulatory advisory

We consolidate your compliance into one unified ingredient-by-market matrix covering the FSSAI, GCC, EU, and US, completely replacing scattered, separate reviews. Simultaneously, we anchor your domestic operations with robust FSSAI product approvals, category classifications, and dynamic regulatory updates—systematically built to withstand heavy scrutiny at every future renewal, not just pass the first check.

FA

Formula & Safety Audit

Comprehensive formulation audits and safety assessments: screening for dosage margins, ingredient interactions, and manufacturability—not just regulatory permission status.

LC

Label compliance

Label-ready submissions and packaging review calibrated to India, GCC, EU, US, and Australia requirements at the same time — not retrofitted market by market after a rejection.

SC

Supply chain advisory

Sourcing and raw-material risk review grounded in ground-level field research — GACP compliance, aflatoxin and contamination risk, NABL-accredited lab verification, and the batch-clubbing issues that quietly derail export consignments.

DD

Regulatory due diligence

Independent assessment of a brand or ingredient's regulatory standing ahead of licensing, distribution, or investment decisions.

Chandrakant Dohare, Founder of Arvena Sciences

Chandrakant Dohare

Founder & Principal Consultant
Arvena Sciences

Founder

Chandrakant Dohare

I operate at a rare, critical intersection: biological sciences, law, applied nutrition, and food processing technology. As the founder of Arvena Sciences, I provide across India as well as international nutraceutical and functional food brands with elite health intelligence, formulation integrity reviews, and airtight regulatory advisory. Before Arvena Sciences existed as a company, this work existed as raw field research. My perspective was shaped by a Field research with the World Bank-funded project in the Gir region of Gujarat, followed by 12+ years of applied health practice and nutritional observation work, with a focus on pediatric immunity and lymphatic function. That ground-level research background — not just regulatory theory — is what shapes how Arvena Sciences reviews a formulation or a supply chain.

Arvena Sciences is a Government of India recognised MSME (UDYAM-GJ-01-0632380), based in Ahmedabad, Gujarat.

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How an engagement runs

A short, predictable process from first enquiry to a filed submission.

Enquiry & scoping

You submit an enquiry through the portal or contact form; we confirm scope and fee within one business day.

Formulation & document review

You upload your formulation and existing documentation through the secure client login portal, we identify gaps against the requirements of every market you're targeting.

Dossier preparation & filing

We prepare the scientific dossier and submission, share drafts for your review through the portal, and file once approved.

Follow-through

We track the submission status and manage any queries from the authority on your behalf.

Ten filters run on every formulation

Most consultancies apply one or two of these well. The edge isn't any single filter — it's that none of them get skipped, because they're built into how the work happens rather than left to whoever happens to be reviewing that day.

The ten filters

Each one screens for something specific most single-market or generalist review misses — and each translates into a concrete edge for the client.

Arvena Sciences 10 Filters Process Infographic

See what we'd find in your formulation

A short, focused look at your product against the markets you've named — two or three real findings, not a sales pitch.

Science & IP

A proprietary ingredient, developed in-house.

Arvena Sciences holds a novel proprietary preparation of Glycyrrhiza glabra (Mulethi), developed through our own formulation research. It's available as a specialty ingredient to strategic partners under commercial NDA. If a licorice-derived active fits your product roadmap, mention it in your enquiry and we'll take the conversation from there.

Client portal

Every engagement runs through a private client portal — not email threads that get lost. Message your consultant directly, track submission status, and exchange documents securely.

Create a client account

Regulatory updates, occasionally

Short notes when FSSAI guidance, GCC label requirements, or export rules change. No noise.