// LEGAL · QUALITY POLICY

The standards
we live by.

Quality is not a department at Athena — it is the operating system for the whole company. This policy documents the principles, certifications and behaviours that make our products worthy of the claims they carry.

ISO 9001ISO 22000HALALKOSHER
Last updated: December 2025

1. Our commitment

Athena Nutrascience Pvt. Ltd. (“Athena”) is committed to delivering evidence-based nutraceutical, biotechnology and life- sciences products that are safe, effective, and consistent — every batch, every market, every time. This Quality Policy defines the principles, standards and behaviours that guide every function of our organisation, from raw-material sourcing to final release.

2. Quality principles

Our quality culture rests on five non-negotiable principles:
  • Evidence first. No claim, formulation or specification enters our line without a defensible dataset.
  • Traceable by design. Every batch carries a full, auditable chain of custody — from botanical source to finished dose.
  • In-house rigour. Analytics, potency and purity testing are performed under our own supervision, not outsourced without oversight.
  • Continuous improvement. We treat every deviation, complaint or observation as an opportunity to strengthen our system.
  • Compliance is the floor, not the ceiling. We meet regulatory standards as a minimum — internal specifications typically exceed them.

3. Certifications & standards

Athena operates in alignment with the following international and Indian quality frameworks:
  • ISO 9001 — Quality Management Systems
  • ISO 22000 — Food Safety Management Systems
  • HALAL — Compliance for global halal markets
  • KOSHER — Compliance for kosher-certified supply chains
Our manufacturing partners and analytical laboratories operate under applicable Good Manufacturing Practice (GMP) frameworks, and all products intended for sale carry the certifications required by their destination markets.

4. Product safety & integrity

Every product we release is designed with three safety layers in mind: raw-material qualification, in-process controls, and finished- product release testing. We verify identity, purity, potency, microbial load, and stability against internal specifications that typically exceed regulatory minimums. Any batch that fails to meet specification is quarantined, root-cause investigated, and destroyed or rejected before it reaches a customer.

5. Raw-material sourcing

We qualify every supplier before onboarding and audit them on a risk-based schedule thereafter. Botanicals, ferment-derived actives, excipients and packaging materials must arrive with a valid Certificate of Analysis and are re-tested in-house before they enter our formulation stream. Adulteration, misidentification, and heavy- metal contamination are treated as automatic rejection criteria.

6. Research & clinical rigour

Formulations progress through discovery, characterisation, bioavailability engineering and validation stages before they are commercialised. Where clinical evidence is claimed, studies are designed with independent statistical review, executed under IRB or equivalent ethical oversight, and reported honestly regardless of outcome. We do not overstate benefits.

7. People & training

Quality is built by people who understand it. Every team member — from bench scientist to warehouse operator — is trained on the elements of this policy relevant to their role, and refresher training is delivered at least annually. Employees are empowered to stop the line if quality is at risk.

8. Complaints & recalls

We maintain a documented complaints and recalls procedure. Every complaint is logged, investigated, and closed with a formal root- cause analysis and corrective/preventive action. Where a batch risk is identified, we have the systems and traceability to execute a market recall efficiently and transparently.

9. Continuous improvement

Our Quality Management System is reviewed by leadership at least annually. Metrics — deviation rate, complaint rate, on-time-in-full release, audit findings — drive the objectives set for each new cycle. This is not a certificate we frame; it is a discipline we practice.

10. Governance

Ultimate accountability for this policy rests with the Founders of Athena Nutrascience. Day-to-day authority is delegated to the Head of Quality, who reports directly to the CEO. This policy is reviewed and republished at least annually or whenever material changes to standards or operations require it.

11. Contact

For questions about this policy, quality documentation, or to request a supplier audit or Certificate of Analysis, write to connect@athenanutrascience.com.

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