Partner with us

You have the product.
We have the Kingdom.

Entering Saudi Arabia is not one job. It is five — registration, importation, licensed storage, institutional listing, and a sales team that already holds the relationships. Most manufacturers assemble that from five suppliers and hope the seams hold. ATHEER PHARMA owns every one of them.

What entry actually requires

Five jobs.
Usually five suppliers.

Each of these has to be done, in order, before your product reaches a patient in the Kingdom. Miss one and the rest stall — and the manufacturer, not the agent, carries the delay.

01 · SFDA REGISTRATION

The file has to exist first

Classification of the product, localisation of the dossier and the filing itself. Until the registration is in place, nothing downstream can legally begin.

02 · IMPORTATION

Someone licensed has to bring it in

Import, clearance and release under a Saudi licence — held by the company whose name is on the registration, not borrowed from a third party.

03 · LICENSED STORAGE

And hold it correctly

Licensed, GDP-aligned storage, temperature-mapped, with a validated 2–8 °C chain for the lines that need one. SFDA licence WL-2023-DR-0043.

04 · INSTITUTIONAL LISTING

Then get onto the lists that buy

NUPCO, the Ministry of Health, the military and security health services, the specialist centres and the private hospital groups — each on its own terms and its own timetable.

05 · A SALES TEAM

That already holds the relationships

People who already sit in front of the hospital pharmacist, the tender committee and the chain buyer. Relationships are not a launch cost that can be skipped.

All five, under one licence.

One company, one contract, one accountable name — not five. Not a broker, not a freight agent, not a reseller.

Start the conversation

What a partner gets

Registered. Planned.
Stocked and delivered.

Three commitments, in the order they happen. Each one is done by our own people, in the Kingdom, under the licence that carries our name.

01 · REGISTRATION OWNED

The people who file are the people you meet

SFDA classification, dossier localisation and filing by our in-house regulatory team — end to end, including variations and listing. You are not handed a consultant's number and a status you cannot check.

02 · LAUNCH PLANNED

A written plan, not an intention

A market analysis and a phased launch plan for your portfolio, in writing: which products go first, which channel opens when, and how the public and private routes are sequenced rather than attempted at once.

03 · STOCKED AND DELIVERED

Our warehouse, our fleet, our date

Licensed storage, a validated 2–8 °C cold chain and delivery into thirteen administrative regions on vehicles we own — which is why the delivery date we give is the one you get.

Medicines Medical devices Food supplements Health products (OTC/GSL) Cosmetics Orphan & unlicensed under SFDA permits
Walk the full route

The market

The largest market
in the region.

Saudi Arabia is the largest pharmaceutical market in the Middle East and North Africa — roughly a third of regional demand, in one country, under one regulator.

SAR 44B

Forecast Saudi pharmaceutical market for 2030

≈33%

Roughly a third of all MENA pharmaceutical demand

35M+

Population, with rising chronic disease prevalence

SAR 44 billion ≈ US$11.8 billion. Source: Daleel, accessed August 2026.

SCALE

One country, one regulator

Regional volume that elsewhere is split across a dozen markets sits here behind a single registration route. The work of entry is done once.

DEMOGRAPHY

Demand that does not switch off

A population above 35 million with rising chronic disease prevalence — sustained demand for chronic therapy, devices and consumer health rather than one-off volume.

VISION 2030

Localisation is policy, not sentiment

Healthcare capacity and local manufacturing are national objectives. A route that is Saudi-licensed, Saudi-staffed and able to point at locally made lines is on the right side of that policy — ours already includes THERAVÉ®, made in Saudi Arabia.

THE REGULATORY FLOOR

Tightening — which helps the licensed

Serialisation and track & trace, enforcement of good distribution practice, stricter registration. Each raises the cost of an improvised route and favours distributors who are already licensed, audited and traceable. We operate RSD track & trace on that basis.

Evidence, not adjectives

The route already runs.

None of this is a proposal. It is the operation as it stands today — and every figure below can be evidenced with the licence, the temperature record, the KPI or the batch trace.

97%

On-time delivery against institutional KPI

40+

Hospitals and medical cities served directly

13

Administrative regions within delivery scope

2–8 °C

Cold chain validated end to end

RSD

Track and trace across the licensed supply chain

Already on this route

Ten manufacturers.

Exclusive and selective agreements across the United States, Europe, the United Kingdom, the GCC and inside the Kingdom.

SyriMedUnited Kingdom
Pharma LineItaly
LogidexItaly
SASMARBelgium
Rhei LifeSerbia
EM PHARMAUnited Kingdom
GAIA PharmaceuticalsUnited Arab Emirates
MedinfarPortugal
i3 PharmaceuticalsUnited States
5MSaudi Arabia · manufacturing
See what a partner gets
One company owns every step
from the factory door
to the hospital shelf.

The distance is our problem, not the customer's. Every route ends at the patient.

Start the conversation

Tell us what you make.

Send the product, the category and the country. If it belongs in this market we will say so and show you the route; if it does not, we will say that too.

Prefer to write directly? Partnership enquiries go straight to coo@atheerpharma.com, or by telephone on +966 13 814 1386. This form reaches the same desk — use whichever suits you.