Frequently Asked Questions

Zanax Health is an integrated pharmaceutical and nutraceutical solutions company offering trading, turnkey projects, R&D, contract manufacturing, regulatory services and strategic advisory.

Our head office is in Ahmedabad, Gujarat, with business and R&D liaison offices in Mumbai and Hyderabad.

Yes. We sign mutual non disclosure agreements before any detailed technical or commercial discussion.

We support shipments to Africa, Southeast Asia, CIS, Latin America and the Middle East, along with selected regulated markets depending on the product registration status.

Yes. We arrange private label and loan licence supply using your artwork, packaging specifications and registration requirements.

Typical documents include COA, COPP, free sale certificate, GMP certificate, packing list, commercial invoice and certificate of origin, based on what the destination country requires.

A typical oral solid dosage facility takes 12 to 24 months from design freeze to commercial production, depending on scale, approvals and site readiness.

Yes. We prepare URS documents, evaluate vendors, attend factory acceptance tests and manage installation and site acceptance.

Absolutely. We carry out gap assessments and plan upgrades that bring existing plants up to current GMP expectations with minimal production downtime.

For fully funded development projects, the formulation and associated data are transferred to the client as agreed in the development contract.

Yes. We develop tablets, capsules, powders, gummies, effervescent formats and liquids for nutraceutical and wellness brands.

Yes. We plan stability protocols for the ICH climatic zones relevant to your target markets, including Zone IVb.

MOQs depend on the dosage form and pack. We work with both startup brands and large distributors and will suggest the most economical batch size.

First orders typically take 30 to 45 days after artwork and sample approval, depending on material availability and batch size.

Yes. Client audits are welcome and we coordinate site visits and quality agreements before commercial production begins.

CTD is the ICH format used by most regulated markets, while ACTD is the ASEAN variant with its own structure for quality, safety and efficacy sections. We prepare both.

Yes. We carry out gap assessments, prepare documentation and SOPs, train teams and support the site during inspection.

Yes. We handle post approval variations, renewals and periodic updates so your registrations remain valid.

Both. We advise promoters, private equity funds, family offices and strategic buyers evaluating opportunities in pharma and nutraceuticals.

Yes. We screen, shortlist and approach suitable partners and targets based on your criteria, while keeping your identity confidential.

Engagements can be retainer based, project based or success fee linked, depending on the scope and nature of the mandate.