Biocompatibility testing service for medical devices compliant with ISO 10993 standards. Evaluates material safety and compatibility with human tissue to support regulatory approval and market clearance for implantable and patient-contact devices.
Manufactured by
IETQAN Conformity and Certification
Cairo, Egypt
IETQAN believes in perfection, and it s not just a name for us; it s our core driver and the code we strive to uphold. Our logo represents the DNA as a symbol of a perfect object, which is what we aim to achieve in everything we do. As an ISO 17025, ISO 17020, ISO 17021 accredited service provider, we ensure that our services meet the highest standards of quality, accuracy, and reliability. Deliver activities that meets the regulatory requirements in ever increasing demanding regulatory environment is key target for our team. Our team of experts is dedicated to providing you with outstanding service, and we strive to exceed your expectations every time IETQAN is proud to offer testing, validation, and technical services to the Medical Devices Pharmaceutical Sectors throughout Egypt and the area. With more than 1500 assignments, and our reports have been reviewed and accepted by many regulatory authorities and noticed bodies.
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Accuprec Research Labs Pvt. Ltd. · India
Comprehensive biocompatibility evaluation for medical devices aligned with ISO 10993 standards and global regulatory requirements. Services include cytotoxicity, sensitization, irritation, and systemic toxicity testing to ensure device safety for patient use.
Jiangsu Kerbio Medical Technology Group Co., Ltd. · China
Comprehensive biocompatibility evaluation services for medical devices and biomaterials, assessing toxicity, sensitization potential, and immune system compatibility in accordance with ISO 10993 standards. Services include material chemical characterization, in vitro cytotoxicity testing, and animal implantation studies.
Applus+ Laboratories · Spain
Biocompatibility testing service evaluates medical device materials and components for safety and compatibility with human tissue. Assesses cytotoxicity, sensitization, irritation, and systemic toxicity to support regulatory compliance and device approval. Supports product development through comprehensive material characterization and standards-based testing protocols.
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