Facilities
Qatar Pharma manufacturing facilities have been designed and built to meet all major international standards and regulations: current Good Manufacturing Practices (cGMP), U.S. Food and Drug Administration (FDA). It is dedicated to self-contained I.V. infusion solution production and quality control facilities, which are completely separated from multipurpose manufacturing facilities.
QC/QA: Qatar Pharma Quality Assurance (QA) system encompasses all current good manufacturing practices (cGMP) including effective quality control (QC) as well as design & development considerations, ISO 9000 and ISO 14001 standard requirements.
LAY-OUT Supervision and management:
The company includes two sectors directly reporting to the Chairman and G.M. these departments is:
- Services sector
- Technical sector
Services sector includes the following departments:
- Information Technology (IT)
- Finance
- Human Resource Department (HRD)
- Water treatment station includes the following:
- Osmotron
- Purified water tank
- Purified water loop
- Pure steam generator
- Distiller (Multitron)
- Water for injection loop
- Water for injection storage tank
- Solution preparation to PE bottle
- Solution preparation to PP bags
- BFS (PE) bottles filling system
- FFS (PP) filling bags system
- SVP (Ampoules & Glass Vials)
- Plastic Factory for packaging material
- Sterilization area include two Autoclave one for PE bottle line and another one of PP bags
- Routine inspection / Self-inspection & claims and Recall
- Validation and Calibration
- Training, Documentation and Batch release
- Release of Finished Products
- Chemical analysis
- Microbial analysis
- Physical analysis
- Environmental Control
- Mechanical
- Electrical
- Civil Instrumental
- Validation and Calibration
- Engineering Projects
- HVAC System
- Raw Material
- Packaging Material
- Finished Products
- Spare Parts
- Chemicals