Pharmaceutical Business Development · Sultanate Of Oman

Your Route To Market In Oman And The Gulf.

We select, register, launch and distribute pharmaceutical products in Oman — and open the path onward to the GCC, the Middle East and Africa.

Biosimilars & Biologics

Biosimilars And Specialty Products, Registered And Launched In Oman.

From immunology to nephrology, we register and distribute biosimilar therapies that give hospitals a quality-assured, cost-effective alternative to originator biologics.

Local Manufacturing

A GMP-Licensed Packaging Line, Inside Oman, Today.

Products packaged locally are priced as Omani production — a 20% price preference, 30% for full local manufacture.

Scroll
15+ Years
Pharmaceutical management and manufacturing experience
3 Products
In registration with the Oman Ministry of Health
GMP
Licensed packaging line at our partner facility in Oman
6 Markets
In the GCC expansion path
The Opportunity

A market that imports almost everything — and pays more for what is made locally.

Oman imports 95.4% of the medicines it uses. It also offers a 30% price preference for locally manufactured products, 20% for products packaged locally, and advance purchase agreements covering up to 30% of Ministry of Health requirements.

Import Share
0%
of Oman's medicines are imported
95.4% imported
Imported 95.4%
Made locally 4.6%
Price Preference
0% / 0%
paid on top of your price for local packaging / local manufacture
+20%
Local Packaging
+30%
Local Manufacture
Market Growth
USD 0bn → 0bn
The GCC pharmaceutical market
20242033
+107% growth
What We Do

Six services. One accountable partner.

Most companies entering Oman assemble a local agent, a regulatory consultant, a distributor and a promotion team separately. We are all four.

01

Portfolio Selection

We assess your product against Oman's tender data and price file, and tell you whether it can win here.

02

Registration

Dossier, eCTD submission, GMP and CPP handling, deficiency responses and pricing committee — as your local agent.

03

Market Access & Pricing

Price file strategy, tender cycles, and the local-manufacture price preferences where your product qualifies.

04

Medical & Pharmacovigilance

Scientific engagement, medical information, and a named pharmacovigilance responsible person.

05

Marketing & Sales

Launch planning, approved promotional material, and coverage of hospitals, clinics and retail pharmacy.

06

Distribution

Import, customs clearance, validated cold chain, stock cover and recall readiness.

Our Process

From First Conversation To First Order.

A clear, five-stage path — with realistic timelines at each step, and no promises we can't keep.

1

Assess

Product, competition and price band.

2–4 Weeks
2

Agree

Agency terms and supply pricing.

4–8 Weeks
3

Register

Dossier, testing, pricing committee.

10–18 Months
4

Launch

Tenders, hospitals, field coverage.

From Month One
5

Grow

Local packaging, then the next GCC market.

Year Two
Realistic Total First Conversation To First Order: ~12–20 Months
Start The Clock

Indicative for Oman. We give a product-specific projection after the assessment, and we do not promise approval dates.

A GMP-licensed packaging line, inside Oman, today.

Through our partner and shareholder Opal Bio Pharma, a product packaged in Oman is treated as locally produced — and priced accordingly by the Ministry of Health. It does not require you to move primary manufacturing or transfer your process. Biotechnology lines follow over the next three years.

How local manufacturing works
GMP LICENSED
In Registration Now

Three products on the path to approval.

All three are under review by the Oman Ministry of Health. Below is where each one sits in the process, and what it will address.

01

Adalix

adalimumab · 40 mg / 0.4 mL
Therapeutic Area Immunology
Reference Product Humira®
Presentation Pre-filled syringe
Registration progress Dossier under review
Immunology
02

Glarise

insulin glargine · 100 U / mL
Therapeutic Area Diabetes
Reference Product Lantus®
Presentation Pre-filled pen
Registration progress Dossier under review
Diabetes
03

Epolix

epoetin alfa · 2,000 / 4,000 IU
Therapeutic Area Nephrology
Reference Product Eprex®
Presentation Pre-filled syringe
Registration progress Dossier under review
Nephrology

All three products are under regulatory review by the Ministry of Health in the Sultanate of Oman and are not approved for sale. This page is intended for healthcare professionals and business partners, not the general public.

Tell us about your product.

Send us the molecule and the markets where it is approved. We will tell you whether it has a route in Oman — including when the answer is no. We reply to every enquiry within three working days.