Spectrace
Sectors

Pharmaceuticals and Health Products

In pharmaceuticals, where a product came from, which batch it belongs to and whether it really is what it claims are three separate questions. Spectrace answers all three with a record.

Where things stand

Can you show the origin of the product at every link of the chain?

From warehouse to pharmacy, from hospital to inspection, responsibility changes hands at every stage. An unbroken record also ends the question of where the problem began.

  • Product entering the chain from outside
  • Matching batch and shipment
  • Cold chain and distribution records
  • Audit and export files
Pharmaceuticals and Health Products

Where the sector stands

In pharmaceuticals a product passes through many hands between manufacturer and patient, and responsibility changes at every stage. Where the record breaks at one of those stages, where the problem began cannot be established afterwards.

Product entering the chain from outside is not only a brand matter but a patient safety matter. Building an identity bound to the product together with a record at unit level narrows both detection time and the scope of intervention.

How Spectrace approaches it

An identity bound to the product and a record bound to the chain.

Mark the product

Grafex and Lumvex place a signature that belongs to you, without adding a visible element to the packaging.

Measure the content

Molevex ties agreement between composition and declaration to a measured record.

Record the chain

Tagvex follows every unit by its own number, matching shipments at unit level.

What you secure

When the record is unbroken, three things fall into place at once.

Patient safety

Product entering the chain from outside is noticed before it reaches a patient.

Regulatory compliance

The traceability an inspection asks for stops being a file you assemble separately.

Corporate responsibility

Which stage the problem arose at is read from the record, so disputes stay short.

Frequently asked

How does it relate to regulatory requirements?

The system is built to produce the traceability information an inspection asks for, so records stop being a file assembled separately.

Can cold chain records be kept too?

Because field readings are written to the central record, data on distribution conditions can be collected in the same flow.

Does rollout stop production?

Rollout proceeds in stages and work on the line is aligned with planned downtime.

Traceability in your pharmaceutical chain

Once your distribution structure is provided, the layers required are assessed on our side.

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