DRAP

Also called: Drug Regulatory Authority of Pakistan

DRAP — The Drug Regulatory Authority of Pakistan — the federal regulator for medicines and medical devices, established under the DRAP Act 2012.

For medical devices, DRAP operates under the Medical Devices Rules, 2017. Devices are classified by risk from Class A (low) to Class D (high), and importers, manufacturers and distributors need the relevant establishment licence.

Buyers should check that a supplier holds a valid licence and that the product itself is enlisted or registered as its class requires.

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