Egypt's Leading Accredited Testing & Validation Laboratory
ISO 17025 and ISO 17020 certified services for medical device manufacturers and pharmaceutical companies across Egypt and the wider Middle East.
Explore Our Services
About IETQAN
Who is IETQAN?
IETQAN is Egypt’s first ISO 17025 and ISO 17020 accredited service provider for medical device and pharmaceutical testing — and the only provider of its kind serving the wider Middle East and Africa region.
With over 20 years of industry experience, our team has completed more than 1,500 testing, validation, and qualification assignments. Every report we issue meets the rigorous expectations of international regulatory authorities and notified bodies. When compliance matters, IETQAN delivers certainty.
Learn More About UsOur Services.
IETQAN Testing Services
Testing Services.
Our accredited laboratory performs a comprehensive range of tests to support medical device and pharmaceutical product safety, regulatory compliance, and market approval.
- Packaging System Testing
- Packaging System Accelerated Aging Studies
- Residual EO/ECH Analysis
- Heavy Metal Testing
- Lubricant Concentration Testing
- Biocompatibility Testing (ISO 10993)
- Microbiological Testing
0+
Years of Experience
0+
Completed Assignments
Highly Rated
Client Satisfaction
ISO 17025 & ISO 17020
Accreditation Status
| IETQAN News |
Our Company believes in perfection, and it’s not just a name for us; it’s our core driver and the code we strive to uphold.
Knowledge Centre
Accelerated Aging Calculator
Use IETQAN's free Accelerated Aging Calculator to determine the required chamber conditioning time for your packaging shelf-life studies, based on the ASTM F1980 method. Enter your target shelf life, ambient temperature (TAA), and real-time temperature (TRT) to calculate your Accelerated Aging Factor (AAF) and chamber conditioning period. For expert guidance on your complete accelerated aging programme, contact our packaging engineers.
Policies & Procedures
Access IETQAN's quality policies and standard operating procedures, developed and maintained in full compliance with ISO 17025 and ISO 17020 requirements. These documents support supplier qualification reviews, client audits, and regulatory inspections.
Technical Forms
Download IETQAN's technical documentation forms for use in testing submissions, project initiation, and regulatory filings. Accurate and complete documentation is fundamental to every assignment we conduct.
Ready to Get Started? Request a Quote.
Tell us about your project and we will respond with a detailed quotation within one business day. Our team is ready to support your compliance goals.
| Our Clients |
