Quality Framework
Our Standards
ALTIOMA is built on transparent formulation, disciplined quality processes, and compliant communication. We design our standards to be verifiable—so partners and customers can trust what’s stated and what’s shipped.
Note: This page describes our operating principles. Specific testing documentation (e.g., COA) is provided per lot when available.
Formulation philosophy
We build formulations with a “clarity first” mindset: transparent ingredients, rational design, and language that stays within compliant boundaries.
Principles
- Clear ingredient disclosure and straightforward labeling.
- Evidence-informed selection of ingredients and forms (where applicable).
- Practical dosing strategy (no gimmick under-dosing by design).
- Compliant positioning: no disease claims, no misleading “miracle” language.
What we avoid
- Proprietary blends used to obscure dosages.
- Marketing-driven ingredient “sprinkles” that can’t be justified.
- Non-verifiable superlatives and medical-style promises.
- Confusing labels that hide important facts.
Manufacturing & quality systems
Our manufacturing expectations are designed to support repeatability, documentation, and consistent execution. Final partner/manufacturer specifics are confirmed per product.
Facility expectations
- Documented quality systems and controlled workflows.
- Batch-level traceability (ingredients → finished product).
- Change control practices where applicable.
- Clear specifications and acceptance criteria.
Documentation mindset
- Lot identifiers and date codes for traceability.
- COA and supporting documents available upon request when applicable.
- Partner-ready paperwork for wholesale workflows.
- Clear communication on any deviations or changes.
Testing & purity approach
Testing should confirm identity, support quality, and reduce avoidable risk. The exact panel can vary by formula and risk profile, but the intent stays the same: verify what matters and document it.
Typical quality checks (example)
- Identity checks (ingredient verification as applicable).
- Microbial screening where relevant.
- Heavy metal screening based on formula and supply chain risk.
- Potency/strength verification where appropriate.
COA availability
- Certificates of Analysis can be provided upon request when available.
- Lot-based references enable partner-level verification.
- We prefer clarity over vague “tested” statements.
- We do not promise panels we cannot deliver.
Label integrity & compliant communication
In supplements, trust collapses when labels and claims get sloppy. We keep messaging within compliant boundaries and avoid exaggeration.
We prioritize
- Clear wording and accurate descriptions.
- Ingredient transparency and rational positioning.
- Responsible, compliant marketing language.
- Consistency across website, listings, and packaging.
We do not do
- Disease claims (explicit or implied).
- “Medical-grade” phrasing without a real, provable basis.
- Before/after style promises or guaranteed outcomes.
- Fear-based or misleading urgency tactics.
Standards FAQ
Short answers, clear boundaries.
When available, COAs can be provided upon request for the relevant lot/batch. Documentation depends on the specific product and manufacturing workflow.
No. Our communication is designed to stay within compliant supplement boundaries and avoid disease-related claims.
Yes. We aim to support partner needs with clean paperwork and traceability where applicable.
Disclaimer: Content on this page is informational and describes internal standards and intent. It is not medical advice.