Portfolio

Five regulated
categories.

Anchored by medicines and medical devices, expanded through consumer health lines, and now extended by our own registered brand. Every category is registered or notified to the SFDA, stored under one licence and delivered on one fleet — which is why a hospital can put all five on a single purchase order.

How to read this page

A category is a route,
not a shelf label.

What a product is decides how it is filed, how it is stored, how it is transported and who may buy it. We classify before we quote.

The words below are used precisely on this site. Where a line is not yet approved we say so, and we do not sell it as if it were.

Registered
Approved and listed with the SFDA. Orderable, stocked and traceable to batch.
Notified
Lodged with the SFDA under the notification route that its category requires.
Under permit
Supplied against a specific SFDA permit — how orphan and unlicensed medicines reach the patient who needs them.
In registration
Filed and under review. We publish the date it is approved, not the date we hope for.

What we distribute

Five categories.
One licence behind all of them.

Filter by the channel you buy through, or read all five.

01 · MEDICINES

Registered, orphan and unlicensed lines

Registered medicines for hospital and retail supply, and hard-to-source specialities brought in under SFDA permits when there is no registered alternative — including orphan products for small patient populations.

Cold-chain and controlled lines are handled inside the same licensed warehouse at 2–8 °C, moved on our own validated vehicles, and traced to batch through RSD.

Registered lines Orphan drugs Unlicensed under permit Cold chain 2–8 °C Controlled lines

Government & NUPCO · Hospitals · Pharmacy

02 · MEDICAL DEVICES

Consumables and devices, hospital and home

Devices and consumables classified, registered and stocked under the same licence as the medicines beside them — so a ward orders the device and the drug on one line, from one supplier, on one schedule.

Device files carry their own evidence requirements. Our regulatory team classifies before it files, which is what keeps a device dossier from being returned for its shape.

THERAVÉ® insulin pen needles 33G pack front — navy artwork marked 33G, 4 mm, Ø0.20 mm, 100 pieces THERAVÉ® insulin pen needles 32G pack front — navy artwork marked 32G, 4 mm, Ø0.23 mm, 100 pieces

Shown: THERAVÉ® insulin pen needles, 33G and 32G — the device line we register and hold ourselves. Partner devices are distributed under the same licence.

Hospital consumables Home-use devices Classified & registered

Government & NUPCO · Hospitals · Pharmacy

03 · FOOD SUPPLEMENTS

Vitamins, minerals and nutraceuticals

Supplied to institutional and retail channels alike, from international manufacturers under agreement and from our own registered range.

THERAVÉ® sits in this category — fifteen SKUs developed for the Saudi market and manufactured in Saudi Arabia to our specification, Halal certified and SFDA registered.

THERAVÉ® Immune C pack front — orange tube artwork, Vitamin C 1000 mg, 20 effervescent tablets THERAVÉ® Hydra Plus carton front — blue artwork, electrolytes plus Vitamin C, 30 sachets × 5 g THERAVÉ® Energy B12 pack front — deep red card artwork, Vitamin B12 1000 µg, 30 oral films

Shown: three THERAVÉ® lines — an effervescent tablet tube, an effervescent sachet carton and an oral film pack.

Vitamins & minerals Nutraceuticals THERAVÉ® own brand

Government & NUPCO · Hospitals · Pharmacy

04 · HEALTH PRODUCTS

OTC and general-sale lines

Over-the-counter and general-sale products registered or notified to the SFDA, moving through pharmacy retail and hospital outpatient pharmacies.

The same storage conditions, the same batch traceability and the same delivery schedule as everything else we hold. Nothing is stored to a lower standard because it is sold without a prescription.

OTC General sale Registered or notified

Hospitals · Pharmacy & retail

05 · COSMETICS

Dermatological and personal care

Dermatological and personal care lines notified to the SFDA and distributed through pharmacy retail, where the counter that sells them is the counter that dispenses the prescription beside them.

Dermatological Personal care Notified to SFDA

Pharmacy & retail

Looking for a specific line?

If it is registered, we can quote it. If it is not, we will tell you what registering it would take and how long it would honestly need.

Ask the desk

Registered & in registration

The portfolio you can order,
and the one arriving.

What is registered today is stocked and orderable today. Behind it sits a pipeline of molecules under active SFDA registration, filed and under review.

We do not publish a count of what is pending, and we do not pre-sell a file that has not been approved. When a certificate is issued, the line appears on the price list and in the warehouse — not before. Partners and institutional customers receive the status of their own files directly, in writing, on the schedule we agreed.

Filed
Dossier localised, assembled and submitted by our own regulatory team.
Under review
Queries answered by the people who wrote the file, not by an intermediary.
Approved
Listed, priced, stocked in Dammam and released to the fleet.
Maintained
Renewals, variations and line extensions tracked against their due dates.

Registration is not a service we buy in. It is a department. See the regulatory desk →

How the portfolio is held

The same standard
behind every category.

A portfolio is only as good as the conditions it is kept in. Ours are documented, and we will show you the record.

A warehouse aisle between tall blue and orange pallet racking, stacked with wrapped and labelled palletised stock on a polished floor
One licensed warehouse in Dammam. Every category on this page is received, released and picked from the same racking, under SFDA licence WL-2023-DR-0043.
A white delivery van in ATHEER PHARMA livery, side profile, parked against the facility building
Our own fleet. More than eight owned vehicles, including validated cold-chain units, carry the portfolio into thirteen administrative regions.
  • One licensed warehouse. Dammam, under SFDA licence WL-2023-DR-0043 — not five depots and not a subcontracted network.
  • GDP-aligned operations. Receiving, storage, picking and release run to good distribution practice.
  • Validated cold chain. 2–8 °C held end to end, warehouse to vehicle to delivery point.
  • Controlled lines. Held and released under the controls their classification requires.
  • RSD track and trace. Batch-level traceability from receipt to the point of delivery.
  • Our own fleet. More than eight owned vehicles, including validated cold-chain units, reaching thirteen administrative regions.
Quality & operations
97%

On-time delivery against institutional KPI

40+

Hospitals and medical cities served directly

2–8 °C

Cold chain validated end to end

13

Administrative regions within delivery scope

Ask for any of it to be evidenced — the licence, the temperature record, the KPI, the batch trace. Everything here is a document, not a claim.

Where the portfolio comes from

Ten manufacturers,
and one brand of our own.

OUR PARTNERS

Exclusive and selective agreements

Ten manufacturers across the United States, Europe, the United Kingdom, the GCC and inside the Kingdom appoint us for this market — one contract, one accountable name, the whole route under a single licence.

See the partners
THERAVÉ®

When the world does not make it, we do

Fifteen SKUs across effervescent tablets, oral dissolving films and effervescent sachets — made in Saudi Arabia, Halal certified and SFDA registered, moving through the same warehouse and fleet as everything else.

See the range

Partner with us

Your product belongs
on this list.

If you manufacture a product that belongs in this market, we provide the full route: regulatory strategy and SFDA registration through to nationwide sales, marketing and distribution — under one accountable name.

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