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Expertise
An experienced team with in-depth knowledge of import regulations, HS classification and clearance procedures.
DRAP documentation · ADC processing
Your trusted partner for DRAP clearance
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.
What this desk clears
What we handle
Every consignment type this desk files, examined and released under the correct regulatory workflow.
We prepare and file DRAP Release Order / Clearance Certificate requests on PSW.
We assemble and verify the licence, invoice, batch and analysis documents DRAP expects.
We follow up directly with the Assistant Drug Controller's office through to issuance.
Guidance on Form 5 drug import licences and Form 6 for test / analysis quantities.
We link DRAP approvals to your Goods Declaration inside the PSW Single Declaration.
Compliance with DRAP's Release Order procedure and the Assistant Drug Controller's review at every step.
DRAP processing is where pharmaceutical shipments are won or lost. The regime is precise: the drug import licence, the Release Order request, the batch and analysis documents and the Goods Declaration all have to agree. A single inconsistency invites a query, and a query invites demurrage. Our sole job here is to make that documentation flawless and to keep it moving.
We work the Pakistan Single Window daily. Since DRAP shifted commercial clearance from OIES to PSW in August 2024, Release Orders are requested inside the Single Declaration and tied to the customs entry. We know the screens, the document checklists and the people, so requests go in complete and come out approved.
Approvals move faster when someone is following them up in person. We maintain active liaison with the Assistant Drug Controller's office, answer queries the same day and escalate where a shipment is time-critical, the difference between a consignment that clears this week and one that sits.
Whether you are a manufacturer importing raw materials, a distributor bringing in finished medicines, or an importer of surgical products and devices, we plug DRAP processing straight into your customs clearance so you deal with one team, not two.
We manage the DRAP side of the clearance so it dovetails with the customs entry.
Our process
We assess your products and confirm the DRAP pathway and documents required.
We prepare the licence, invoice, COA and supporting documents.
We file the Release Order / Clearance Certificate request on the Single Window.
We liaise with the Assistant Drug Controller and resolve any query quickly.
The Release Order is issued and linked to your GD for customs clearance.
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
In trade parlance, ADC processing refers to obtaining DRAP's import authorisation through the Assistant Drug Controller, today issued as a Release Order / Clearance Certificate on PSW. We prepare the request, submit it and follow it through the ADC's review to issuance.
Since 15 August 2024, DRAP clearance of commercial imports at Karachi Seaport and Airport is processed on the Pakistan Single Window. The Release Order is requested inside the PSW Single Declaration and linked to your Goods Declaration.
We guide you on the Form 5 drug import licence and Form 6 for test / analysis quantities, and we make sure your licence covers the items you intend to import before a shipment is booked.
Both. DRAP processing is most valuable when it is joined to the customs filing, we handle the Release Order and the Goods Declaration together so there is no gap between approval and release.
By filing complete requests, answering ADC queries the same day and escalating time-critical consignments. Most delays are documentation errors, which we remove before submission.
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.
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.
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.