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Expertise
An experienced team with in-depth knowledge of import regulations, HS classification and clearance procedures.
Finished medicines · Import clearance
Your trusted partner in finished-medicine imports
Customs clearance for finished pharmaceutical medicines in every dosage form, tablets, capsules, syrups, injectables and biologicals, with DRAP registration checks, Release Order processing and careful, timely handling.
What this desk clears
What we handle
Every consignment type this desk files, examined and released under the correct regulatory workflow.
Clearance of solid oral dosage forms, registered brands and generics.
Clearance of oral liquids, suspensions and topical preparations.
Priority, temperature-aware clearance of injectables, vaccines and biologicals.
We verify DRAP registration and secure the Release Order on PSW before release.
We reconcile batch numbers, manufacturing and expiry dates against the declaration.
Compliance with DRAP product registration and Import Policy Order conditions on every consignment.
Finished medicines can only be imported by holders of the relevant DRAP registration or marketing authorisation, and every consignment needs a Release Order before customs will let it go. We check that the products on your invoice match a valid registration, then file and pursue the Release Order on PSW so the two move in step.
Where you need to bring in an unregistered or not-available medicine, we advise on the documentation route DRAP permits and manage the additional approvals involved, a pathway that rewards experience and close follow-up.
Injectables, vaccines and biologicals do not tolerate delay or heat. We prioritise these consignments, push examination through quickly and coordinate temperature-controlled onward delivery, so shelf life and cold chain are protected from terminal to warehouse.
Batch numbers, manufacturing and expiry dates are reconciled against your declaration up front, a small discipline that avoids the value and batch queries that most often hold medicine shipments at the port.
Finished drugs are cleared under DRAP registration with Pakistan Customs.
Our process
We review invoice, packing list, B/L, LC and DRAP registration details.
We confirm the products are registered / permitted and prepare the PSW submission.
We request and follow up the DRAP Release Order through the Assistant Drug Controller.
We file the GD on WeBOC/PSW once the Release Order is in hand, then manage assessment and examination.
Medicines are released and delivered under the right conditions to your location.
Why choose us
An experienced team with in-depth knowledge of import regulations, HS classification and clearance procedures.
We ensure 100% compliance with Pakistan Customs and every relevant regulatory authority, DRAP, DPP, PTA and more.
We value your time, an efficient WeBOC/PSW process that keeps clearance and delivery on schedule.
From documentation and OGA approvals to delivery, we handle everything with professional care.
A commitment to quality that has earned us the trust of valued importers across Pakistan.
FAQ
As a rule, finished medicines must be DRAP-registered and imported by the registration holder. Unregistered or not-available drugs can be imported through a specific DRAP-permitted route with additional documentation, which we can manage for you.
Yes, therapeutic goods need a DRAP Release Order before customs release. We request it on PSW and follow it through the Assistant Drug Controller to issuance, timed to your shipment's arrival.
We prioritise clearance of injectables, vaccines and biologicals, expedite examination and arrange temperature-controlled delivery so the cold chain and remaining shelf life are preserved.
Commercial invoice, packing list, Bill of Lading / Airway Bill, LC (if applicable) and your DRAP registration details. We tell you exactly what is missing before the goods arrive.
Most holds trace to a value or batch mismatch, an incomplete Release Order or an HS-code question. Our pre-arrival check is designed to remove these before the consignment lands.
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.
Specialist DRAP documentation and ADC processing, we prepare, file and follow up the Release Order on the Pakistan Single Window so your therapeutic goods clear customs without avoidable delay.
Customs clearance for surgical products, medical devices, diagnostic kits and healthcare equipment, with DRAP Medical Devices compliance, import NOC processing and dependable release.
Get started
Get in touch with our expert team today for a quick, compliant and competitive quote.