Trust & transparency

Quality & Manufacturing

By NeuroPouch Team Updated May 2026
The short version

NeuroPouch is manufactured in the European Union under GMP, notified to the relevant national food-supplement authority, and produced in batches that are tested for identity, potency and contaminants before release. Every tin carries a batch code that traces back to ingredient suppliers and Certificates of Analysis (COAs).

Manufacturing

NeuroPouch is produced at an EU-based contract manufacturing facility specialising in oral pouch and supplement formats, operating under Good Manufacturing Practice (GMP). GMP is the recognised manufacturing standard for food supplements and pharmaceuticals in the EU and the UK; it covers premises, equipment, personnel hygiene, raw material controls, in-process checks, finished-product testing, documentation, and traceability.

Regulatory framework

Testing

Each production batch is tested for:

Traceability

Every tin and tower carries a batch number printed on the packaging. The batch number links to:

Customers and trade partners can request a batch's COA package by emailing quality@getneuropouch.com with the batch code from the tin.

Storage and shelf life

Each tin carries a best-before date. Store in a cool, dry place away from direct sunlight. Keep out of reach of children. Do not consume if seal is broken or tin is damaged on receipt.

Recalls and adverse-event reporting

If a quality issue is identified that would affect consumer safety, NeuroPouch operates a recall procedure consistent with Regulation (EC) 178/2002 traceability obligations. Adverse events should be reported to quality@getneuropouch.com with batch code, product, and a description of the incident. Suspected serious reactions should also be reported to the national food-safety authority of the consumer’s member state.

Contact

Quality, batch COA, technical questions: quality@getneuropouch.com.