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Middle East

Importing medicines into Oman

Regulator, legal routes, documents, approval times and shipping lanes for medicines supplied from India to Oman.

At a glance

Regulator
DSC
Main route
Import of a non-registered drug through a licensed warehouse
Courier transit from India
2 to 5 days
Air cargo transit from India
3 to 8 days

Short answer

Medicines in Oman are regulated by the Ministry of Health through its Drug Safety Center. An unregistered medicine enters through the Ministry's non-registered drug import service, filed by a licensed pharmaceutical warehouse for a public or private health institution, and each consignment then needs Ministry release at the port before it reaches the hospital.

Research summary, confirm with the regulator or a local agent

This guide was researched from official and published sources. A regulatory specialist has not confirmed it yet, so check current requirements before you rely on it.

Content updated November 13, 2026

Key facts

Regulator
Ministry of Health, Drug Safety Center (DSC)
Main route
Import of a non-registered drug through a licensed warehouse
Who applies
Licensed pharmaceutical warehouse in Oman, acting for a public or private health institution
Import permit or approval
Needed before goods ship
Supply addressed to patients
Not a legal route. Supply goes to a licensed consignee
Typical approval time
The Ministry of Health lists about one week for the non-registered drug import service and one working day for customs release. Plan 1 to 3 weeks for the regulatory steps in total and confirm the current timeline with the Drug Safety Center.
Courier transit from India
2 to 5 days
Air cargo transit from India
3 to 8 days
Common Incoterms
CIP, DAP, FCA
Local currency
OMR
Languages
Arabic, English

Legal routes and who applies

Routes for a medicine that is not registered in Oman. The local party named under each route files the application, not the exporter.

  1. Route 1About one week (Ministry of Health service page)

    Import of a non-registered drug through a licensed warehouse

    A Drug Safety Center e-service that lets a licensed pharmaceutical warehouse import an unregistered medicine for the private or public sector. The applicant needs a licensed warehouse and a purchase licence, and the Ministry lists no fee. The Ministry's Circular No. 17 of 2024 implements a guideline for importing non-registered medicine, which sets the detailed conditions.

    Who applies: Licensed pharmaceutical warehouse in Oman, acting for a public or private health institution

  2. Route 21 working day (Ministry of Health service page)

    Customs release and release to market

    Every consignment needs Ministry approval for customs release and a no-objection to sale. The commercial invoice must be certified by the source and show batch numbers and manufacture and expiry dates, and a certificate of analysis is required. The fee is 5 rials per imported batch.

    Who applies: Licensed pharmaceutical company or warehouse represented by an Omani pharmacist

  3. Route 37 working days for the transport licence (Ministry of Health service page)

    Controlled drug import permit and transport licence

    An import permit for narcotic or psychotropic substances is requested through the Ministry e-portal, and a separate transport licence must be issued against every import or export permit for such items. Oman's narcotics law is the Narcotics and Psychotropic Control Act No. 17 of 1999 with its executive regulations.

    Who applies: Licensed establishment that imports narcotic or psychotropic medicines

  4. Route 4Released on arrival

    Personal medicines carried by travellers

    Travellers bring personal medicines with a medical report or prescription issued within six months by the treating institution. Controlled medicines are released for up to one month of use and non-controlled medicines for up to three months. This is a travellers' rule, not a route for parcels sent by a supplier.

    Who applies: The traveller, or a relative or representative carrying the medicine

Document checklist

Documents a buyer in Oman usually needs. The exact list depends on the route and the product.

  • Ministry of Health approval to import the non-registered drug, issued to the licensed warehouse
  • Purchase licence and the hospital's purchase request or local purchase order
  • Physician request describing the patient need and the lack of a registered alternative
  • Commercial invoice certified by the source, with batch numbers and manufacture and expiry dates
  • Certificate of analysis for each batch
  • Certificate of pharmaceutical product or proof of registration in the country of origin
  • GMP certificate for the manufacturing site
  • Biological or plasma certificate for biological products
  • No-objection certificate and transport licence for controlled drugs
  • Packing list and air waybill

The documents a country, buyer type and product usually need, ready to print.

Build a checklist for your request

The regulator

The Ministry of Health regulates medicines in Oman through its Drug Safety Center (DSC), which registers products, licenses pharmaceutical establishments and approves imports and customs release. Older Ministry documents use the name Directorate General of Pharmaceutical Affairs and Drug Control (DGPA&DC), and both names still appear in current material. Applications are filed through the Ministry's e-Health portal, and each DSC service page lists its documents, fee and completion time.

Supply to public hospitals and to private facilities runs through licensed pharmaceutical warehouses. The DSC publishes its rules as numbered circulars, so a buyer should check the latest circulars before relying on any older guidance.

The starting point is that a medicine must be registered and the importing company licensed. The DSC clearance service lists a registered drug and a registered company among its conditions, so an unregistered medicine needs its own approval first.

Non-registered drug import service

The Ministry runs an Import of Non Registered Drug e-service. It lets a business import an unregistered medicine through a licensed pharmaceutical warehouse, for both the private and the public sector. The applicant must hold a licensed warehouse and a purchase licence. The service has no fee and a listed completion time of about one week. The detailed conditions sit in a guideline brought into force by Circular No. 17 of 2024, dated 1 January 2024.

A 2019 law firm overview by Al Tamimi describes the earlier practice: special permission to import an unregistered product on a named-patient basis where a specific patient needs it and no suitable product is on the local market. The same overview reports that a non-registered medicine may be accepted in a public tender when its price is more favourable. Both points should be checked against the 2024 guideline.

Customs release

After approval, each batch needs DSC customs release and a no-objection to sale. The service takes one working day and costs 5 rials per batch. The invoice must be certified by the source and show batch numbers and dates, and the company's representative must be an Omani pharmacist. Biological products need a biological or plasma certificate.

Controlled medicines

Narcotic and psychotropic medicines need an import permit through the e-portal and a transport licence against every import permit, listed at 7 working days. Clearance also needs a no-objection certificate. The Indian export side needs its own controlled-drug authorisation.

Travellers

The Ministry's travel guidance allows a traveller to bring personal medicines with a medical report or prescription issued within six months, up to one month of use for controlled medicines and three months for others. It does not describe a route for a supplier to post medicines to a patient.

Documents a buyer usually needs

  • Ministry approval for the non-registered drug, issued to the licensed warehouse
  • Purchase licence and the hospital's purchase request or local purchase order
  • Physician request explaining the patient need and why no registered product is suitable
  • Commercial invoice certified by the source, showing batch numbers and manufacture and expiry dates
  • Certificate of analysis for each batch, a GMP certificate and proof of registration in the country of origin
  • Biological or plasma certificate where relevant
  • No-objection certificate and transport licence for controlled drugs
  • Packing list and air waybill

Timeline: a worked example

A hospital in Muscat needs a medicine for a named patient. The medicine is not registered in Oman.

Step Who acts Typical time
Physician request and hospital purchase request Treating physician and hospital pharmacy 1 to 3 days
Proforma invoice, certificate of analysis and GMP evidence Exporter in India 2 to 5 days
Non-registered drug import approval Licensed warehouse with the DSC About 1 week, longer if the DSC raises queries
Export documents and dispatch from India Exporter and forwarder 2 to 7 days, longer if a CDSCO export NOC is needed
Direct flight to Muscat Carrier 1 day
DSC customs release and delivery DSC, customs and the warehouse 1 to 3 days

Total: roughly 2 to 4 weeks from request to delivery. These are planning estimates, not published service times.

Shipping lanes from India

Muscat (MCT) has direct flights from Mumbai, Delhi, Chennai, Hyderabad, Bengaluru and several Kerala airports, and Salalah (SLL) has a smaller number of direct routes. Express courier service is usually 2 to 5 days door to door for small, non-controlled parcels. Air cargo is usually 3 to 8 days including DSC release. Sea freight from Mundra or Nhava Sheva to Sohar or Salalah is a short lane for ambient tender volumes, but air remains the normal mode for named-patient and cold-chain supply.

CIP and DAP are the usual terms, and FCA suits warehouses with their own forwarder. DDP is rarely practical because the Omani warehouse holds the approval and clears the goods.

Practical tips for buyers

  • Agree early which licensed warehouse will file the non-registered drug request, since the route runs through a warehouse rather than the hospital itself.
  • Make sure the supplier certifies the commercial invoice by stamp or signature, a stated condition for release.
  • Duty on HS 3004 medicines is 0 percent according to World Bank WITS data for the GCC common tariff.
  • Oman's standard VAT rate is 5 percent. From 1 October 2026, Tax Authority Decision No. 224 of 2026 sets the list of zero-rated medicines and medical equipment, replacing Decision No. 59 of 2021, and zero-rating depends on Ministry of Health clearance.
  • Excess quantities brought in by travellers are destroyed under Ministry supervision, so personal supply should stay within the stated limits.

Shipping from India at a glance

Typical transit times and terms on the lanes from Indian airports to Oman.

Courier, door to door

2 to 5 days

Air cargo with clearance

3 to 8 days

Usual Incoterms

CIPDAPFCA

Cold chain on this lane

Muscat is about three hours by air from western India and has frequent direct flights, so transit is short. From May to September ground temperatures in Muscat often pass 45°C, so use passive shippers qualified for a summer profile, data loggers and pre-booked cool-room storage, and agree who holds the goods while the Ministry release is issued.

Check a shipper against this lane

Transit times are typical estimates from India, not carrier commitments.

Questions about importing into Oman

Who regulates medicine imports in Oman?

The Ministry of Health regulates medicines through its Drug Safety Center, which approves imports, customs release and pharmaceutical establishment licences. Older documents use the name Directorate General of Pharmaceutical Affairs and Drug Control.

Can an unregistered medicine be imported into Oman?

Yes, through the Ministry's Import of Non Registered Drug service. A licensed pharmaceutical warehouse applies for a public or private health institution, with a purchase licence, and the Ministry lists about one week for the approval. Circular No. 17 of 2024 brought the current guideline into force.

How long does Ministry release take when the goods arrive in Oman?

The customs release service is listed at one working day and costs 5 rials per batch. The invoice must be certified by the source and show batch numbers and expiry dates.

Can a patient in Oman receive prescription medicine directly from a supplier abroad?

No published route allows this. The Ministry's personal-use rules cover travellers carrying their own medicines, and unregistered medicines are imported through a licensed warehouse for a health institution, so a patient should ask the treating physician or hospital.

What duty and VAT apply to imported medicines in Oman?

World Bank WITS data shows 0 percent duty on HS 3004 medicines under the GCC common tariff. The standard VAT rate is 5 percent, and from 1 October 2026 Decision No. 224 of 2026 lists the medicines that are zero-rated, subject to Ministry of Health clearance.

How are controlled medicines imported into Oman?

The importer requests an import permit for narcotic or psychotropic substances through the Ministry e-portal and obtains a transport licence for each permit, listed at 7 working days. Clearance also needs a no-objection certificate.

Sources

Official sources first, then published secondary sources. Each was read when this guide was researched.

  1. 1.Ministry of Health Oman, Import of Non Registered Drug service
  2. 2.Ministry of Health Oman, Customs release and release of medicines to market
  3. 3.Ministry of Health Oman, Circular No. 17 of 2024 on the guideline for importing non-registered medicine
  4. 4.Ministry of Health Oman, Licence to transport narcotic and psychotropic substances
  5. 5.Ministry of Health Oman, Medications and travel
  6. 6.World Bank WITS, Oman MFN tariff on HS 300490 (TRAINS 2023)
  7. 7.Lookuptax, Oman zero-rate decisions 223 to 225 of 2026
  8. 8.PwC Worldwide Tax Summaries, Oman other taxes (reviewed July 2026)
  9. 9.Al Tamimi, Pharmaceutical registration in Oman, an overview (2019)

This page explains how regulatory routes work. It is not legal or medical advice. Confirm current requirements with the regulator or a local agent before goods ship.

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