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A Personal Health Application (PHA) tool contains a patient's personal data (name, date of birth and other demographic details). It also includes a patient's diagnosis or health condition and details about the various treatment/assessments delivered by health professionals during an episode of care from a health care provider. It contains an ...
Portable Document Format (PDF), standardized as ISO 32000, is a file format developed by Adobe in 1992 to present documents, including text formatting and images, in a manner independent of application software, hardware, and operating systems.
The Requirements Modeling Framework (RMF) is an open-source software framework for working with requirements based on the ReqIF standard. RMF consists of a core allowing reading, writing and manipulating ReqIF data, and a user interface allowing to inspect and edit request data.
Different file systems have different limits on the depth of the filename path, creating potential problems and limitations based on the file system hierarchy in use. [10] Thirdly, with respect to the use of the TMF Reference Model as a database schema, the TMF RM v3.0 spreadsheet cannot be used without manual modification as a classification ...
An electronic trial master file (eTMF) is a trial master file in electronic (digital content) format.It is a type of content management system for the pharmaceutical industry, providing a formalized means of organizing and storing documents, images, and other digital content for pharmaceutical clinical trials that may be required for compliance with government regulatory agencies.
an Office suite; allows to export (and import, with accuracy limitations) PDF files. Microsoft Word 2013: Proprietary: Desktop software. The 2013 edition of Office allows PDF files to be converted into a format that can be edited. Nitro PDF Reader: Trialware: Text highlighting, draw lines and measure distances in PDF files. Nitro PDF Pro ...
A biologics license application (BLA) is defined by the U.S. Food and Drug Administration (FDA) as follows: The biologics license application is a request for permission to introduce, or deliver for introduction, a biologic product into interstate commerce (21 CFR 601.2). The BLA is regulated under 21 CFR 600 – 680.
In the United States, once obtaining the appropriate medical degree, physicians can apply to attain licensure via Board certification. In India, practitioners of both modern medicine and traditional medicine are subject to professional regulation.