Building local pharmaceutical excellence

A medium-scale facility focused on high-demand generic medicines, strengthening the Kingdom's drug security.

Building local pharmaceutical excellence

USD 15 Million

Total project investment

50-70 Million

Units per year

2,000-3,000 m2

Planned facility area

24-30 Months

Estimated implementation

USD 7+ Billion

Saudi pharmaceutical market size

7-9%

Estimated market growth

80%+

Import dependency in the Kingdom

25-30%

Annual ROI after year two

Product portfolio

Four therapeutic categories at launch

Anti-diabetic

Anti-diabetic

  • Metformin
Cardiovascular

Cardiovascular

  • Atorvastatin
  • Amlodipine
Gastrointestinal

Gastrointestinal

  • Omeprazole
Analgesics and anti-inflammatories

Analgesics and anti-inflammatories

  • Paracetamol
  • Ibuprofen

Fifteen million in, and what it returns

USD 12-18M

Annual revenue potential

35-40%

Gross profit margin

20-25%

EBITDA margin

5-7 Years

Payback period

Full breakdown
Land and building
USD 4.5M
Machinery and equipment
USD 6.0M
Utilities and installation
USD 1.0M
Raw material inventory
USD 2.0M
SFDA registration and consultancy
USD 0.5M
Initial marketing and salaries
USD 1.0M
Total capital expenditure
USD 11.5M
Working capital and pre-operational
USD 3.5M
Annual EBITDA potential
USD 3-5M

The incentive environment, by benefit type

Tax

Corporate tax
0% up to 20 years
Effect
Higher long-term returns

Financing

Potential SIDF financing
75% of project cost
Effect
Reduced equity requirement

Procurement

Government price preference
10-15%
Effect
Advantage in public tenders

Duty

Exemption value
USD 300K-500K
Applies to
Imported machinery and raw materials

Twenty-four to thirty months to commercial launch

  1. 6 months

    Planning and approvals

    Manufacturing licence and product registration with SFDA.

  2. 12 months

    Design and construction

    Facility build to GMP specification.

  3. 6 months

    Procurement and installation

    Machinery delivery, installation and qualification.

  4. 6 to 12 months

    Regulatory and commissioning

    GMP compliance, pre-approval inspection and validation studies.

  5. Operations begin

    Commercial launch

    First commercial batches released to market.

A healthier future for Saudi Arabia

  • Healthcare localisation under Vision 2030
  • Import dependency reduction across essential medicines
  • Skilled job creation and economic growth
  • Stronger national drug security