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Medical Device
Specific-Non-Active Devices
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Medical Device
Medical Device / General
Medical Device / Specific-Active Devices
Medical Device / Specific-Non-Active Devices
Medical Device / Accreditation
Medical Device / Forum
Certificates
Certificates / EN ISO 13485 Quality Management System
Certificates / TS EN ISO / IEC 17025 General requirements for the competence of testing and calibration laboratories
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S24. Orthopedic and Maxillofacial Cement and Graft
S32. Ceramic Manufacturing techniques and formation processes
S54. Non-implantable devices for anaesthesia, emergency and intensive care, Production technologies, characterization and quality control, safety and efficacy requirements based on conformity assessment approach, specific standards and guidelines.
S55. Non active non implantable ophthalmologic devices, quality control, safety and efficay requirements for conformity assessment, specific standards and guidelines
S18. nanomaterial & nanotechnology production technologies, characterization ,safety and efficay requirements
S11. Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
S16. Chemical and Biological Indicators
Importance and Basic Requirements of Water Systems/Su Sistemlerinin Önemi ve Temel Gereklilikleri
Requirements for aseptic processing of medical devices , EN 556-2, EN ISO 13408 series based on conformity assessment approach
Devices for anaesthesia, emergency and intensive care-Non Implantable
Ethylene oxide-Sterilization of healthcare products
MDR conformity assessment activities for Non-Active Implantable devices-Experience Sharing
Requirements for the development, validation and routine control of moist heat sterilization process for medical devices (EN ISO 17665) with conformity assessment approach
Vaporized Hydrogen Peroxide- Low temperature sterilization
Alloy heat treatment processes and their effect on material characteristics with conformity assessment approach, risk based characterization and quality control tests
Biodegradable Materials and Devices
S23. Biomaterial: Fundamentals and Applications
S40. Cardiovascular, Vascular, Neurovascular implants production technologies - specific production technologies - characterization and quality control, safety and efficacy requirements based on conformity assessment, specific standards and guidelines
S35.Cardiovascular, Vascular, Neurovascular non implantable devices, production technologies - characterization and quality control, safety and efficacy requirements based on conformity assessment, specific standards and guidelines
Cleanrooms and associated controlled environments
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