検査用語集 | H - N
「H」から始まる用語
「I」から始まる用語
I&A→IARC→ICD→ICMJE→ICMJEUR→ICNIRP→ICRP→ICSH→ICT→ICU→ICタグ→IDSC→IEC→IEC/TR60513 : Fundamental Aspects of Safety Standards for Medical Electrical Equipment→IEC60601-1 : Medical Electrical Equipment - Part 1 : General Requirements for Basic Safety and Essential Performance→IEC60601-1-2 : Medical Electrical Equipment - Part1-2 : General Requirements for Safety – Electromagnetic Compatibility - Requirements and Tests→IEC62304 : Medical Device Software - Software Life Cycle Processes→IEC62366-1 : Medical Devices - Part1 : Application of Usability Engineering to Medical Devices→IFCC→IFMBE→IHC→IHR→IMDRF→IME→in vitro→in vivo→IOM→IQC→IS→ISO→ISO 11135 : Sterilization of Health Care Products - Ethylene Oxide→ISO 11137-1 : Sterilization of Health Care Products — Radiation Part 1: Requirements for Development、 Validation and Routine Control of a Sterilization Process for Medical Devices→ISO 11137-2 : Sterilization of Health Care Products — Radiation Part 2 : Establishing the Sterilization Dose→ISO 13485 : Medical Devices - Quality Management Systems - Requirements for Regulatory Purposes→ISO 14000シリーズ→ISO 15189 : Medical Laboratories - Particular Requirements for Quality and Competence→ISO 15190 : Medical Laboratories - Requirements for Safety→ISO 15195 : Laboratory Medicine - Requirements for the Competence of Calibration Laboratories using Reference Measurement Procedures→ISO 17511 : In Vitro Diagnostic Medical Devices - Requirements for Establishing Metrological Traceability of Values Assigned to Calibrators, Trueness Control Materials and Human Samples→ISO 17665-1 : Sterilization of Health Care Products - Moist Heat Part 1 : Requirement for the Development, Validation and Routine Control of a Sterilization Process for Medical Devices→ISO 18153 : In vitro Diagnostic Medical Devices - Measurement of Quantities in Biological Samples - Metrological Traceability of Values for Catalytic Concentration of Enzymes Assigned Calibrators and Control Materials→ISO 18362 : Manufacture of Cell-based Health Care Products - Control of Microbial Risks during Processing→ISO 19011 : Guidelines for Auditing Management Systems→ISO 31000 : Risk Management – Guidelines→ISO 5725-1 : Accuracy(Trueness and Precision) of Measurement Methods and Results — Part 1 : General Principles and Definitions→ISO 5725-2 : Accuracy(Trueness and Precision) of Measurement Methods and Results − Part 2 : Basic Method for the Determination of Repeatability and Reproducibility of a Standard Measurement Method→ISO 9000 : Quality Management System - Fundamentals and Vocabulary→ISO 9000シリーズ→ISO 9001 : Quality Management Systems – Requirements→ISO 9004 : Managing for the Sustained Success of An Organization - A Quality Management Approach→ISO Guide 35 : Reference Materials − General and Statistical Principles for Certification→ISO/IEC 17021 : Conformity Assessment - Requirement for Bodies Providing Audit and Certification of Management Systems→ISO/IEC 17025 : General Requirements for the Competence of Testing and Calibration Laboratories→ISO/IEC 17043 : Conformity Assessment − General Requirements for Proficiency Testing→ISO/IEC Guide 43-1 : Proficiency Testing by Interlaboratory Comparisons - Part1 : Development and Operation of Proficiency Testing Schemes→ISO/IEC Guide 43-2 : Proficiency Testing by Interlaboratory Comparisons - Part2 : Selection and use of Proficiency Testing Schemes by Laboratory Accreditation Bodies→ISO/IEC Guide 98-3 : Uncertainty of Measurement - Part3 : Guide to the Expression of Uncertainty in Measurement(GUM)→ISO TC→ISR→IU→IUPAC→i.v / IV→IVD→IVDD→IVD MD→