About us
Who is IETQAN?
IETQAN is Egypt’s first — and the region’s leading — ISO 17025 and ISO 17020 accredited service provider for medical device and pharmaceutical testing, validation, and technical services. Our accreditation spans Egypt, the Middle East, and Africa, and our reports are recognised and accepted by international regulatory authorities and notified bodies worldwide.
Our name embodies our mission. The DNA helix in our logo represents the fundamental building block of perfection — a symbol of our commitment to precision, reliability, and scientific rigour in everything we do. For over 20 years, we have supported manufacturers, importers, and distributors of medical devices and pharmaceutical products in demonstrating that their products meet the highest international standards of safety and quality.
Whether you need a single test report to satisfy a regulatory submission or a comprehensive validation programme for a new manufacturing facility, IETQAN brings the expertise, accreditation, and infrastructure to deliver results you can rely on.
Why Choose IETQAN?
Four reasons our clients trust us with their most critical compliance challenges.
Integrated Solutions
We offer end-to-end testing, validation, and certification services under one roof — so you deal with a single accountable partner rather than coordinating across multiple providers. From packaging integrity testing to full sterilizer validation, our integrated approach reduces complexity and accelerates your time to market.
Regional Pioneer in Accreditation
IETQAN was the first organisation in Egypt, the Middle East, and Africa to achieve both ISO 17025 (testing laboratory) and ISO 17020 (inspection body) accreditation. This dual accreditation is not a formality — it is an independent, third-party verification that our technical competence meets the highest global standards.
Clients of All Sizes
We work with organisations across the full spectrum — from early-stage start-ups seeking their first regulatory clearance to the world’s largest multinational pharmaceutical and medical device companies. Whatever your scale, you receive the same rigorous service and the same quality of documentation.
Deep Industry Knowledge
Our team combines decades of hands-on experience in medical device and pharmaceutical standards with practical knowledge of the regional regulatory landscape. We understand the requirements of EDRMP, international notified bodies, and global pharmacopoeias — and we build that knowledge into every assignment we conduct.
Values & Code of Conduct
Our operations are governed by clear values and a published code of conduct. These commitments define how we work with our clients, protect their data, and maintain the independence that makes our reports trusted by regulators worldwide.
IETQAN Values
- Integrity and ethics in all activities
- Impartial counsel and unbiased validation outcomes
- Customer focus — your compliance goals are our goals
- Shared knowledge and continuous professional development
- Full transparency in reporting and communication
Code of Conduct
- We keep the interests of our clients as our highest priority.
- We accept only those assignments we are qualified to perform.
- We refuse all assignments in which we have a conflict of interest.
- We adhere to and maintain the professional standards required by our accreditation bodies.
- We act with good faith, honesty, and fairness in all professional dealings.
- We respect the confidentiality of all business and personal information shared with us.
- We deliver professional, independent, and unbiased advice.
- We issue reports that are accurate records of actions taken, in full alignment with our best practices and accreditation requirements.