Drug Delivery Systems Testing Service

Chemical analysis and testing service for medical device materials and components to ensure safety and compliance. Performed by accredited laboratory following international quality standards.

Comprehensive rheological testing and characterization service for medical creams, gels, injectable suspensions and biopharmaceutical formulations. Supports product development, process optimization and method validation with custom protocols and expert consultation.

Comprehensive testing and validation of dialyzers, hemofilters, and adsorbents for regulatory submission. Ensures compliance with DIN EN ISO 8637 series standards for extracorporeal devices.

Comprehensive performance evaluation and validation platform for medical materials and devices through standardized testing protocols and real-world optimization.

Laboratory analysis service for medical device quality, safety, and microbiological validation. This service ensures compliance with ISO 13485 and regulatory requirements.

Comprehensive service supporting development of diagnostic devices from concept through manufacturing. Includes platform selection, process optimization, and scale-up support. Bridges gap between R&D and regulated production.

Expert service providing surface characterization and specialized coatings for optimized dispensing performance. Supports processing of difficult materials and novel biomaterials. Enables enhanced functionality of diagnostic devices.

Comprehensive pharmaceutical development service utilizing organ chip platforms for preclinical efficacy and toxicity assessment. Covers early discovery through clinical trial preparation phases.

Water quality analysis service for medical device manufacturing and processing. Ensures compliance with pharmaceutical and medical device quality standards.

Professional calibration service ensuring accurate testing and measurement of medical devices. Maintains traceability to national standards and supports regulatory compliance.

Physicochemical performance testing service for medical devices and biomedicines, including preclinical research, material characterization, and regulatory compliance testing. Supports manufacturers in validating device safety, efficacy, and quality parameters before clinical trials and market registration.

Medical device packaging testing service that validates packaging integrity, sterility barriers, and shelf-life stability for regulated medical products. Ensures compliance with ISO 11607 and FDA requirements through laboratory analysis and performance validation. Supports product safety and regulatory clearance for medical device manufacturers.