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ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.
The sub-clause 4.2.3 of ISO 13485:2016 requires a manufacturer of medical device to establish a Technical file, similar to a device master record. The EU medical device regulation requires a manufacturer of a medical device to maintain a Technical documentation.
A design history file is a compilation of documentation that describes the design history of a finished medical device.The design history file, or DHF, is part of regulation introduced in 1990 when the U.S. Congress passed the Safe Medical Devices Act, which established new standards for medical devices that can cause or contribute to the death, serious illness, or injury of a patient.
The Medical Devices Directive (MDD 93/42/EEC) similarly lists several requirements regarding the design of a medical device. The Medical Devices Regulation (MDR (EU) 2017/745), replacing the MDD from 2021, requires information to allow the design stages applied to the device to be understood as part of the design and manufacturing information ...
ISO 13482:2014 Robots and robotic devices – Safety requirements for personal care robots; ISO 13485:2016 Medical devices – Quality management systems – Requirements for regulatory purposes; ISO/IEC 13490 Information technology – Volume and file structure of read-only and write-once compact disk media for information interchange
ISO 13485:2016, Medical devices - Quality management systems - Requirements for regulatory purposes ISO 16000-40 :2019, Indoor air - Part 40: Indoor Air Quality Management System ISO/TS 17582 :2014, Quality management systems - Particular requirements for the application of ISO 9001:2008 for electoral organizations at all levels of government
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