The standard we hold
every batch to.
We don't operate a factory floor — so our quality framework has to do more work, not less. This is how a formulation earns the right to carry the Qazivo name, end to end.
The formulation process
Research & hypothesis
Every formulation starts with a review of published clinical and pre-clinical literature on candidate actives, dose ranges and delivery formats.
Formulation design
Ingredient sourcing grade, excipients, dosage strength and delivery format (capsule, powder, gummy, liquid) are specified in a written formulation brief.
Partner qualification
The brief is matched to a licensed, GMP-certified manufacturing partner, audited against our quality checklist before any production run is approved.
Batch release testing
Every production batch is tested by an independent, accredited laboratory against potency, purity and safety parameters before it is released for sale.
Our manufacturing-partner framework
Every contract manufacturer we work with is qualified, and re-audited, against this framework.
| Domain | Requirement | How it's verified |
|---|---|---|
| Licensing | Valid FSSAI manufacturing license (or applicable regional equivalent), plus category-specific approvals. | Document verification & renewal tracking |
| Manufacturing practice | Current Good Manufacturing Practice (GMP) certification for the facility and product category. | Certificate review + facility audit |
| Food/quality management | ISO 22000 or HACCP-aligned quality management system in place. | Certification review |
| Raw material traceability | Certificates of Analysis on file for every raw material lot, traceable to source. | Batch documentation audit |
| Finished-batch testing | Potency/assay, heavy metals, microbial load and (where relevant) pesticide residue testing per batch. | Independent, accredited third-party laboratory |
| Stability | Shelf-life supported by real-time or accelerated stability data appropriate to the format. | Stability dossier review |
| Labelling accuracy | Declared claims and nutrient values match tested values within regulatory tolerance. | Cross-check against lab Certificate of Analysis |
Nothing ships on trust alone.
Batch release testing is performed by laboratories independent of the manufacturing partner. A batch that fails any parameter is rejected — it does not reach a Qazivo package, regardless of cost already incurred.
We publish the parameters we test for below in the interest of being legible to partners, retailers and regulators alike — not as a substitute for the underlying Certificate of Analysis, which is maintained on file per batch.
Request our QA documentation →Regulatory alignment
Frameworks differ by market. We design formulation dossiers to anticipate that, rather than react to it.
India
Formulated with reference to FSSAI's Food Safety and Standards (Health Supplements, Nutraceuticals...) Regulations, and manufactured only by appropriately licensed facilities.
Export markets
Formulation dossiers are structured to support ingredient-legality and labelling review for GCC, Southeast Asian, UK and North American markets ahead of entry.
Claims discipline
Structure/function language is substantiated against cited literature before use, and adapted to what each market's regulator permits.