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Trust & Safety

High standards, quality you can verify

Trust is not a tone of voice. It is a chain of documents that connects a raw material to the batch code on the product in your hand.

Sourced ✦ Tested ✦ Documented

The Standard

One quality system, three product types

A serum, a capsule and a care sensor have almost nothing in common technically. They have everything in common in how we govern them.

Every material we buy is qualified before use. Every manufacturing partner is audited. Every finished batch is verified by a laboratory with no interest in the answer. Every claim on a label is traceable to a document we can produce on request.

When something fails, it does not ship. That sounds obvious; in an industry with launch dates and marketing calendars, it is the single hardest commitment to keep — which is why we put the authority to stop a release with quality, not with commercial.

Controls

What we check, and when

Supplier qualification

Audits, certificates of analysis, and documented chain of custody. Suppliers who cannot evidence origin do not become suppliers.

Incoming materials

Identity and potency confirmation on arrival — because a certificate is a claim until it is verified.

GMP manufacturing

Production in facilities operating to current Good Manufacturing Practice, with batch records retained and reviewable.

Contaminant screening

Heavy metals, microbial limits and, where relevant to the material, pesticide and solvent residues on the finished batch.

Label accuracy

Independent confirmation that what is declared on the panel is what is in the product, at the amount stated.

Stability & shelf life

Real-time and accelerated stability establishing the date after which we no longer stand behind the product.

Transparency

What you are entitled to ask us

These are not favours. If a company cannot answer them, that is your answer.

  • The complete ingredient list, in descending order, with function stated
  • The concentration of any active we make a claim about
  • Where a key raw material is sourced and how it is verified
  • Which laboratory performed the finished-batch testing
  • What a product is not suitable for, and who should avoid it
  • How to reach a person about an adverse reaction, and what happens next

Certification marks, registrations and testing partners are published as each product line is released, so that what appears here can always be checked against a real document.

Safety Reporting

If something goes wrong

Adverse reactions are rare and they still happen. How a company behaves in that moment is the whole measure of it.

01

Stop and report

Discontinue use and contact us at [email protected] with the product, batch code and what you experienced. Seek medical attention for anything severe.

02

We investigate

Reports are logged, the batch is reviewed against its retained sample and release documentation, and we tell you what we find — including when we find nothing.

03

We act

Where a batch or formulation is implicated, we withdraw it. Reformulation and recall are treated as functioning quality systems, not as embarrassments to manage.

Quality & Safety

Documentation available on request

Retail buyers, clinics and distributors can request our quality documentation pack before placing a first order.