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This technical information report (TIR) should be regarded as a reference for developing safe software systems to be used in medical devices. The information that it contains provides a framework within which experience, insight, and judgment are applied systematically to...
This document specifies a set of methods, headers, and properties composing Web Distributed Authoring and Versioning (WebDAV) SEARCH, an application of the HTTP/1.1 protocol to efficiently search for DAV resources based upon a set of client-supplied criteria.
First published in 2001: This handbook has been written to give those professionals working in the development and use of medical devices practical knowledge about biomedical technology, regulations, and their relationship to quality health care. Author: Richard C. Fries
Purpose This standard defines the life cycle requirements for MEDICAL DEVICE SOFTWARE. The set of PROCESSES, ACTIVITIES, and TASKS described in this standard establishes a common framework for MEDICAL DEVICE SOFTWARE life cycle PROCESSES. Field of...
Purpose This standard defines the life cycle requirements for MEDICAL DEVICE SOFTWARE. The set of PROCESSES, ACTIVITIES, and TASKS described in this standard establishes a common framework for MEDICAL DEVICE SOFTWARE life cycle PROCESSES.
This specification defines an extension to Web Distributed Authoring and Versioning (WebDAV) that allows efficient synchronization of the contents of a WebDAV collection.
This document defines extensions to the Web Distributed Authoring and Versioning (WebDAV) protocol to specify a standard way of accessing, managing, and sharing contact information based on the vCard format.
For designers of medical devices, the FDA and ISO requirements are extremely stringent. Designers and researchers feel pressure from management to quickly develop new devices, while they are simultaneously hampered by strict guidelines. The Six Sigma philosophy has solved this...
Web Distributed Authoring and Versioning (WebDAV) consists of a set of methods, headers, and content-types ancillary to HTTP/1.1 for the management of resource properties, creation and management of resource collections, URL namespace manipulation, and resource locking (collision avoidance)....
This specification extends the Web Distributed Authoring and Versioning (WebDAV) Protocol to support the server-side ordering of collection members. Of particular interest are orderings that are not based on property values, and so cannot be achieved using a search protocol's ordering option...
This document specifies a set of methods, headers, and resource types that define the WebDAV (Web Distributed Authoring and Versioning) versioning extensions to the HTTP/1.1 protocol. WebDAV versioning will minimize the complexity of clients that are capable of interoperating with a variety...
Software developer and author Karen Hazzah expands her original treatise on device drivers in the second edition of Writing Windows VxDs and Device Drivers. The book and companion disk include the author's library of wrapper functions that allow the progr Author:...
This document specifies a set of methods, headers, message bodies, properties, and reports that define Access Control extensions to the WebDAV Distributed Authoring Protocol. This protocol permits a client to read and modify access control lists that instruct a server whether to allow or...
The book introduces flexible and stretchable wearable electronic systems and covers in detail the technologies and materials required for healthcare and medical applications. A team of excellent authors gives an overview of currently available flexible devices and thoroughly...
This document applies to any software used in device design, testing, component acceptance, manufacturing, labelling, packaging, distribution and complaint handling or to automate any other aspect of a medical device quality system as described in ISO 13485. This...
This document applies to any software used in device design, testing, component acceptance, manufacturing, labelling, packaging, distribution and complaint handling or to automate any other aspect of a medical device quality system as described in ISO 13485. This...
5.1 A critical step in preparing a medical device for safe use on the next patient is effective cleaning. Typically cleaning a medical device includes precleaning at the point-of-use, manual and automated methods for removing soil that accumulate during clinical use. The...
