GxP-aligned manufacturing
Our in-house production processes support the documentation requirements of pharmaceutical quality systems.

Pharmaceutical packaging sits at the intersection of patient safety and regulatory obligation. In the UK, the Medicines and Healthcare Products Regulatory Agency (MHRA) and EU Falsified Medicines Directive (FMD) requirements mandate tamper-evident packaging across a broad range of prescription and over-the-counter medicines. Non-compliance is not a commercial risk. It is a regulatory and patient safety failure.
Protectaseal manufactures tamper-evident tapes and labels for pharmaceutical manufacturers and packaging operations that require documented, auditable compliance. Every product is manufactured in-house in our secure Devon facility, with full batch traceability, specification documentation, and the serialisation capability that pharmaceutical serialisation programmes demand.

Tamper-evident tapes and labels for folding cartons, blister wallets, and outer packaging.
Sealing labels for pharmaceutical vials, multi-dose bottles, and injection systems.
Unique sequential identifiers with barcode or 2D matrix code for track-and-trace programmes.
Adhesive compounds that maintain temper-evident function across cold and frozen storage conditions.
Tamper-evident labels for investigational medicinal products requiring audit trail documentation.

Our in-house production processes support the documentation requirements of pharmaceutical quality systems.
Every production run is traceable from raw material to finished product.
Custom pharmaceutical specifications are developed and held in strict confidence.
For supply chains requiring demonstrable UK origin and a short, auditable supply chain.
Variable data printing supports pharmaceutical track and trace and FMD compliance programmes.
For pharmaceutical specification enquiries, technical data sheets, or to locate an authorised distributor supplying the pharmaceutical sector, contact our technical team.
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Our tapes and labels are manufactured using GxP-aligned processes with full batch traceability and specification documentation. We support pharmaceutical serialisation programmes and FMD (Falsified Medicines Directive) compliance requirements. Contact our technical team for details on specific regulatory standards.