Al-Qassim Industrial Complex
From Materials to Medicines
We Make It Happen
Our journey begins with raw materials and ends with a trusted pharmaceutical product
The Core Responsibilities of Our Department
01
Warehouse management
We operate through a comprehensive system that has been developed and implemented according to the highest global standards in pharmaceutical warehouse management. This system is characterized by:
- Precise management of material receipt
- Execution of preliminary inspection procedures
- Storage of materials in compliance with global quality standards
- Adherence to Good Manufacturing Practices (GMP)
02
Production Planning and Inventory Control
We consider production planning and inventory control to be among the most essential pillars of supply chain management. We focus on:
- Meeting demand without shortages or excess inventory
- Reducing production and storage costs
- Efficient use of resources (materials, labor, equipment)
All of this is achieved through an accurate production plan that integrates with intelligent and continuously updated inventory control systems
03
Artworks and Packaging Design
We lead the process of designing Artworks & Packaging to ensure
- Full compliance with regulatory requirements
- Professional and attractive product presentation
- Ease of use and clarity of information for consumers
We ensure that the packaging reflects SPIMACO’s identity and fosters customer trust in its products.
04
Contract Manufacturing Organization (CMO)
We manage contract manufacturing operations through well-established collaboration models that ensure:
- Organizing the relationship between SPIMACO and product owners
- Strict adherence to agreed-upon manufacturing specifications
- Protection of intellectual property
- Ensuring quality and full compliance with local and international regulations
Smarter Systems
Stronger Performance
At SPIMACO, innovation isn’t just a goal, it’s how we operate
we implemented transformative technologies that redefined our planning, forecasting, and operational agility, setting a new standard for excellence in pharmaceutical manufacturing.
Key Technologies & Innovations
Enhanced production planning and demand forecasting through advanced algorithms and real-time data integration.
Matirls management through SAP S/4 HANA ERP
Overcame key operational hurdles to implement a smarter, faster ERP system, improving MRP, workflow, and data visibility.
Production Department
Over Two Billion
Therapeutic Units Annually
The role of the Production is to drive operational excellence across seven key Units:
- High Potent
- Oral Solids
- Antibiotics
- Semi-Solids
- Sterile
- Oral Liquids
- Antiseptics
Oral Solid Unit
This Unit for the development and manufacturing of semi-solid dosage forms, such as:
- Tablets
- Capsules
- Dry syrup
A key responsibility is to maintain strict compliance with:
Good Manufacturing Practices (GMP)
Authority Regulation
SFDA
Oral Solid Unit plays a critical role in delivering high quality pharmaceutical solutions through:
Compliance with pharmaceutical standards
Authority Regulation
Continuous process improvement
Sterial Unit
Responsible for the development and manufacturing of sterile manufacturing of:
- Biosimilars
- Prefilled syringe
- Ampules
To guarantee the highest level of product sterility & safety, this Unit ensures:
Compliance with pharmaceutical standards
Authority Regulation
Continuous process improvement
Oral Liquids Unit
From formulation to production & quality control this Unit ensures high-quality manufacturing & seamless packaging of:
- Oral solutions
- Syrups
- Suspensions
Compliance with pharmaceutical standards
Authority Regulation
Continuous process improvement
High Potent Unit
The Unit specializes in the manufacturing of high potent tablets and capsules, focusing on targeted cancer treatments and other critical diseases.
This Unit operates under:
- Advanced safety protocols
- Stringent containment measures
- Strict compliance with international high potent manufacturing standards.
By adhering to these rigorous guidelines, we ensure the highest levels of patient safety and the effectiveness of treatments.
Antibiotics Unit
Responsible for the development and manufacturing of solid dosage forms, such as:
- Tablets
- Capsules
- Dry syrups
A key responsibility is to oversee the production and quality control of penicillin antibiotics, ensuring:
Compliance with pharmaceutical standards
Authority Regulation
Continuous process improvement
Semi-Solids Unit
Responsible for the development and manufacturing of semi-solid dosage forms, such as:
- Gels
- Suppositories
- Ointments
- Creams
This Unit focuses on:
Compliance with pharmaceutical standards
Authority Regulation
Continuous process improvement
Antiseptic Unit
Responsible for the development and production of:
- Antiseptic solutions
- Topical germicidal products
- Disinfectants
To support infection control and hygiene initiatives, they ensure: