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A guide to implementing and maintaining a medical device QMS

WebThe illustrated guide to implementing and maintaining a medical device quality management system. Implementing a medical device quality management …

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An illustrated guide to medical device software development

WebThe illustrated guide to medical device software development and IEC 62304. The IEC 62304 standard includes requirements for managing the life cycle of medical device …

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A guide to software as a medical device, IEC 82304-1 and AI

WebSoftware as a medical device, SaMD, is in the scope of the health software definition and part of the lower left box in the image below. The purpose of the IEC …

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A guide to risk management for medical devices and ISO 14971

WebThe illustrated guide to risk management for medical devices and ISO 14971. Risk management for medical devices refers to the process of ensuring that medical devices …

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A guide to quality management for medical devices and ISO 13485

WebThe illustrated guide to quality management for medical devices and ISO 13485. Quality management for medical devices refers to the systems and processes put in place to …

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Clinical investigation and clinical evaluation MedicalDeviceHQ

WebThe difference lies in the definitions: a clinical investigation is a new study using a medical device in patients to demonstrate the safety and performance of that …

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General Safety and Performance Requirements of the MDR

WebWhen placing a medical device or in-vitro diagnostic medical device on the EU market, it is mandatory to fulfil the General Safety and Performance Requirements …

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What is new in the IEC 62366-1 AMD1:2020

WebFebruary 22, 2022. All articles, Usability engineering 62366-1. In June 2020, the IEC 62366-1 standard underwent some updates. The video below will go over the main changes …

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Medical device software risk management and IEC 62304 …

WebWith our medical device software course selection, you can choose between Software for Medical devices and IEC 62304 and SaMD, IEC 62304 and IEC 82304-1 …

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What is good clinical practice (GCP)

WebGood clinical practice is defined as. “an ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve human subjects. It …

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Usability engineering and risk management for medical devices

WebISO 14971, the risk management standard, defines safety as. “freedom from unacceptable risk.”. ISO 14971:2019, 3.26. In terms of usability engineering and the IEC …

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Creating a medical device work breakdown structure

WebThe WBS (work breakdown structure) is a hierarchical decomposition of the total scope of work to be carried out by the project team to accomplish the project objectives and …

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Authorised representatives, importers and distributors under MDR

WebThe European Commission (EC) is the executive branch of the European Union and it is responsible for enforcing EU laws, directing the EU’s administrative operations, and …

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An alternative approach may be used if

WebRecommendations for Developing User Instruction Manuals for Medical Devices Used in Home Health Care. This guidance was written prior to the February 27, 1997 …

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Buy and download the IEC 62366-1:2015 standard as PDF

WebEN 62366:2008. is the European version of the first issue. It is a harmonised standard with the Medical Device Directive (93/42/EEC). IEC 62366-1:2015. In practice, …

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