Our Core Services
Comprehensive pharmaceutical facility solutions designed to address every aspect of your cleanroom and manufacturing requirements with unmatched expertise and regional knowledge.
Clean Room Design & Construction
ISO 14644 compliant cleanrooms from Grade A to Grade D, designed and constructed to meet GMP requirements with complete contamination control systems and environmental monitoring.
- ISO 14644 Compliance
- GMP-Certified Environments
- Grade A-D Cleanrooms
- Contamination Control
- Environmental Monitoring
- Complete Documentation
MEP Systems Integration
Advanced mechanical, electrical, and plumbing systems designed for pharmaceutical facilities, including HVAC with HEPA filtration, precise environmental control, and backup power systems.
HVAC & Filtration
Advanced HVAC systems with HEPA filtration, precise temperature and humidity control, differential pressure management
Backup Systems
Redundant power systems, emergency generators, UPS systems for critical equipment protection
Water Systems
Purified water distribution, pharmaceutical-grade piping, complete validation documentation
Building Management Systems
Integrated building automation and control systems providing real-time monitoring, automated environmental control, regulatory compliance logging, and energy optimization.
- Real-Time Monitoring
- Automated Controls
- Compliance Logging
- Energy Optimization
- Alarm Management
- Remote Access
Validation Services
Complete validation protocols ensuring regulatory compliance and reliable performance. Our comprehensive IQ/OQ/PQ services provide the documentation required by health authorities.
Installation Qualification (IQ)
Verification that equipment and systems are installed correctly according to specifications
Operational Qualification (OQ)
Confirmation that systems operate within specified parameters across their operating ranges
Performance Qualification (PQ)
Demonstration that systems consistently perform as intended under actual production conditions
Equipment Solutions
Supply and integration of pharmaceutical manufacturing equipment for all dosage forms, including solid, liquid, injectable, and semi-solid production systems.
- Solid Dosage Equipment
- Liquid Production Systems
- Injectable Manufacturing
- Semi-Solid Equipment
- Laboratory Setup
- Analytical Instruments
Pharmaceutical-Grade Water Systems
Complete water purification and distribution systems meeting USP, EP, and pharmacopeial standards for purified water and water for injection applications.
Purified Water Systems
Multi-stage purification including RO, EDI, UV sterilization, and 0.2μm filtration
Water for Injection (WFI)
Distillation or hot water systems meeting pyrogen-free requirements for injectable products
Validation & Documentation
Complete validation protocols, ongoing monitoring, and regulatory compliance documentation
Our Project Delivery Methodology
Turnkey EPC (Engineering, Procurement, Construction) services delivering projects on time and within budget.
Planning & Design
- Requirements Analysis
- Conceptual Design
- Detailed Engineering
- Regulatory Planning
Engineering & Procurement
- Detailed Specifications
- Equipment Selection
- Vendor Qualification
- Material Procurement
Construction & Installation
- Site Preparation
- System Installation
- Quality Control
- Progress Monitoring
Validation & Commissioning
- IQ/OQ/PQ Execution
- Performance Verification
- Training Programs
- Documentation Handover
Compliance & Standards
All our solutions meet international pharmaceutical standards and regional regulatory requirements.
ISO 14644
Cleanroom Classification & Testing
GMP
Good Manufacturing Practice
USP/EP
Pharmacopeial Standards
MENA Regulations
Regional Health Authorities
Ready to Start Your Pharmaceutical Project?
Contact our team to discuss your cleanroom and facility requirements.
Do you have any questions?
Feel free to send us your questions or request a free consultation.