
Expertise
An experienced team with in-depth knowledge of import regulations, HS classification and clearance procedures.
APIs & excipients · Import clearance
Your trusted partner in API & excipient imports
Customs clearance for active pharmaceutical ingredients (APIs) and excipients, the raw materials your manufacturing depends on, with DRAP documentation, correct HS classification and reliable, on-time release.

What this desk clears
What we handle
Every consignment type this desk files, examined and released under the correct regulatory workflow.
Clearance of APIs and drug substances for tablet, capsule, liquid and injectable manufacturing.
Clearance of binders, fillers, solvents, coatings and other excipients used in formulation.
Clearance of primary and secondary pharmaceutical packaging materials imported with your inputs.
We apply online for the DRAP clearance certificate for raw and packaging materials via PSW.
Correct HS-code classification and duty / sales-tax assessment to protect your landed cost.
Compliance with the DRAP raw-material clearance route and correct HS classification of manufacturing inputs.
For a pharmaceutical manufacturer, a delayed API shipment is a stalled batch. Pakistan imports the large majority of its active ingredients, mainly from China and India, so raw-material clearance sits directly on your production critical path. We treat it that way, filing DRAP raw-material clearance certificates promptly and reconciling every certificate of analysis, batch number and quantity against the declaration.
Because APIs and excipients are classified and dutied differently from finished drugs, getting the HS code right matters to both compliance and cost. Our team classifies each item correctly, applies the right assessment and flags any concessionary treatment your inputs may qualify for.
DRAP requires a clearance certificate for raw and packaging materials, applied for online with the requisite documents. We prepare that submission, link it to your Goods Declaration on PSW and carry it through the Assistant Drug Controller's review, so the paperwork is clean and the certificate is ready when the vessel arrives.
The result is fewer queries, less demurrage and a predictable, repeatable clearance you can plan production around, shipment after shipment.
APIs, excipients and packaging materials are cleared under DRAP with Pakistan Customs.
Our process
We collect your invoice, packing list, B/L, COA and manufacturing licence.
We file the online clearance-certificate request for raw / packaging materials on PSW.
We follow up the Assistant Drug Controller review to issuance.
We file the GD on WeBOC/PSW with the raw-material clearance certificate, then handle assessment and examination.
Cleared inputs are delivered to your manufacturing facility on schedule.
Why choose us
FAQ
Raw and packaging materials are cleared against an online DRAP clearance certificate applied for through PSW, backed by your valid manufacturing / import licence. This is distinct from the registration route for finished drugs. We handle the raw-material certificate end to end.
Yes. We clear the full basket of manufacturing inputs, active ingredients, excipients and primary/secondary packaging, under one coordinated filing where they arrive together.
By classifying each item under the correct HS code, applying the right duty and sales-tax treatment, and identifying any concession your inputs qualify for. You get a landed-cost estimate before we file.
Absolutely. For manufacturers running continuous import programmes we standardise the documentation and pre-check each shipment, so clearance becomes predictable and timed to your production schedule.
Usually a COA/batch mismatch, an incomplete DRAP certificate or an HS-code query. Our pre-arrival review is built specifically to catch these before the goods land.
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Get in touch with our expert team today for a quick, compliant and competitive quote.