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CPL|17 October 2018

Product Serialisation for Software and Hardware

CPL is serialisation-ready, in compliance with the Drug Quality Security Act (DQSA).

CPL is serialisation-ready, in compliance with the Drug Quality Security Act (DQSA).

Though compliance was not mandatory until November 2017, the company was ahead of the curve to ensure its products are traceable according to US Food and Drug Administration (FDA) standards.

I addition, the company has invested in a serialisation strategy for both software and hardware systems to support its partners’ serialisation requirements with an ongoing strategy for aggregation as new traceability laws take effect.

Isopropyl myristate (IPM) is widely used as a penetration enhancer and emollient in topical formulations.
Gas chromatography (GC) is a typical chromatographic method used to separate and quantitatively determine analytes that can be volatised without decomposition.
CPL develops and manufactures non-sterile liquid and semi-solid pharmaceutical products. We are solely focused on these dosage forms and have built our reputation as an...
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