+90 532 350 81 15 Contact You

    Hizmetler

    EU 2017/745 MDR Medical Device Regulation

    EU 2017/745 MDR Medical Device Regulation
    Biological Evaluation of Medical Devices

    Biological Evaluation of Medical Devices
    Chemical Characterization

    Chemical Characterization
    Clinical Evaluation

    Clinical Evaluation
    Quality Management Systems

    Quality Management Systems
    Process Validations IQ-OQ-PQ

    Process Validations IQ-OQ-PQ
    PRRC Service

    PRRC Service
    GMP, GDP, GLP Consulting

    GMP, GDP, GLP Consulting
    FDA, UKCA, MDSAP

    FDA, UKCA, MDSAP
    Risk Analysis

    Risk Analysis