We make healthcare
Understandable, Accessible and Affordable.
Our Manufacturers
Our Production flow
Raw Material Import
All Steripharm suppliers are verified to assure strict compliance with ISO 13485 manufacturing standards, guaranteeing quality of all raw materials to be in accordance with CE standards.
Validation & Logging
Upon arrival, all raw materials are inspected individually, and all forms of batch traceability records are created for regulatory inspections.
Manufacturing: Assembly & Intermediary work
All products are manufactured in ISO class 8 certified cleanrooms, adhering to ISO 13485 standards, assuring & minimal chance of any bacterial growth/contamination.
All Steripharm cleanrooms are built to have:
- state-of-the-art air handling system
- air filtration specificity of minimum 5(microns) sized particles
- temperature controlled at 24 +- 3degrees
- HEPA filtration vents
- Positive pressure maintained at 0.01”
Quality assurance: Sterilization and Bio-Burden Testing
All Steripharm sterilizing machines are approved to ISO 1135 standards, fortifying quality assurance compliance with ISO 13485 standards.
Quality assurance practices at Steripharm:
- all individual products are sterilized to assure minimum SAL 1 x 10(-6)
- quarterly bio-burden tests to maintain an acceptable limit of 100 CFU
- in house microbiology lab providing routine maintenance
Packing
All products are packed in ISO cleanroom facilities to assure 0% chance of contamination of any kind.
Supply
With coordinating 6+ storage units throughout the UAE, all with efficient HVAC systems built in Steripharm promises delivery of goods in a timely manner with no cost on product shelf-life or quality.