ISO TR 17302 Nanotechnologies - Framework for identifying vocabulary development for nanotechnology applications in human healthcare - First Edition
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- IEC TS 62607-4-1 Nanomanufacturing – Key control characteristics – Part 4-1: Cathode nanomaterials for nano-enabled electrical energy storage – Electrochemical characterisation, 2-electrode cell method - Edition 2.0
- 07
- CEN EN 16348 Gas infrastructure - Safety Management System (SMS) for gas transmission infrastructure and Pipeline Integrity Management System (PIMS) for gas transmission pipelines - Functional requirements
- ISO 14001 CORR 1 Environmental management systems — Requirements with guidance for use — TECHNICAL CORRIGENDUM 1 - Deuxieme Edition
- SNV SN EN 16348 Gas infrastructure - Safety Management System (SMS) for gas transmission infrastructure and Pipeline Integrity Management System (PIMS) for gas transmission pipelines - Functional requirements
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- ISO 9001 Quality management systems — Requirements - Fifth edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 9001 Quality management systems — Requirements - Fifth edition
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- SNV SN EN 16348 Gas infrastructure - Safety Management System (SMS) for gas transmission infrastructure and Pipeline Integrity Management System (PIMS) for gas transmission pipelines - Functional requirements
- ISO 14001 CORR 1 Environmental management systems — Requirements with guidance for use — TECHNICAL CORRIGENDUM 1 - Deuxieme Edition
- ISO 14001 CORR 1 Environmental management systems — Requirements with guidance for use — TECHNICAL CORRIGENDUM 1 - Deuxieme Edition
- SNV SN EN 16348 Gas infrastructure - Safety Management System (SMS) for gas transmission infrastructure and Pipeline Integrity Management System (PIMS) for gas transmission pipelines - Functional requirements
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- ISO 9001 Quality management systems — Requirements - Fifth edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 9001 Quality management systems — Requirements - Fifth edition
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- SNV SN EN 16348 Gas infrastructure - Safety Management System (SMS) for gas transmission infrastructure and Pipeline Integrity Management System (PIMS) for gas transmission pipelines - Functional requirements
- SNV SN EN 16348 Gas infrastructure - Safety Management System (SMS) for gas transmission infrastructure and Pipeline Integrity Management System (PIMS) for gas transmission pipelines - Functional requirements
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- ISO 9001 Quality management systems — Requirements - Fifth edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 9001 Quality management systems — Requirements - Fifth edition
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- CEN EN ISO 14001 Environmental management systems - Requirements with guidance for use
- ISO 9001 Quality management systems — Requirements - Fifth edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 9001 Quality management systems — Requirements - Fifth edition
- DIN EN ISO 13485 Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- ISO 14644-6 Cleanrooms and associated controlled environments — Part 6: Vocabulary - First Edition
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- IEEE 62659 Nanomanufacturing – Large scale manufacturing for nanoelectronics
- IEC PAS 62565-2-1 Nanomanufacturing – Material specifications – Part 2-1: Single-wall carbon nanotubes – Blank detail specification - Edition 1.0
- ISO TS 80004-1 Nanotechnologies — Vocabulary — Part 1: Core terms - First Edition
- ISO TS 80004-1 Nanotechnologies - Vocabulary - Part 1: Core terms - Second Edition
- Картотека зарубежных и международных стандартов
International Organization for Standardization
Nanotechnologies - Framework for identifying vocabulary development for nanotechnology applications in human healthcare - First Edition
N TR 17302
Annotation
This Technical Report will not attempt a formal, comprehensive definition of “nanomedicine”. Instead, it will provide a taxonomic framework for the development of vocabulary for clinical applications of nanotechnologies in human healthcare. While it is understood that the origins of nanotechnologies for healthcare applications emerge from pre-clinical and translational research, the interest of this Technical Report is to determine where these technologies will impact the clinical value chain and the practice of medicine.
This Technical Report is intended to facilitate communications between developers and users of nanotechnologies, deliverers and users of medicine including the pharmaceutical, research and medical communities, regulatory professionals, and additional organizations and individuals who might interact with these groups, including biotechnology, diagnostic, and medical device companies, the life sciences, patent attorneys and patent offices, institutional review boards, ethics review boards, and accreditation organizations.
Автоматический перевод:
Нанотехнологии - Структура для идентификации развития словаря для применений нанотехнологий в человеческом здравоохранении - Первый Выпуск
Этот Технический отчет не будет делать попытку формального, всестороннего определения “наномедицины”. Вместо этого это будет служить таксономической основой для развития словаря для клинических применений нанотехнологий в человеческом здравоохранении. В то время как подразумевается, что происхождение нанотехнологий для приложений здравоохранения появляется из преклинического и переводного исследования, интерес этого Технического отчета состоит в том, чтобы определить, где эти технологии повлияют на клиническую цепочку создания ценности и практику медицины.



