Search results
Results From The WOW.Com Content Network
Good documentation practice (recommended to abbreviate as GDocP to distinguish from "good distribution practice" also abbreviated GDP) is a term in the pharmaceutical and medical device industries to describe standards by which documents are created and maintained.
Software documentation is written text or illustration that accompanies computer software or is embedded in the source code. The documentation either explains how the software operates or how to use it, and may mean different things to people in different roles. Documentation is an important part of software engineering. Types of documentation ...
Documentation is an integral part of the cycle of inquiry - observing, reflecting, documenting, sharing and responding. [13] Pedagogical documentation, in terms of the teacher documentation, is the "teacher's story of the movement in children's understanding". [13]
Google Developer Documentation Style Guide, published online by Google. [17] Provides a set of editorial guidelines for anyone writing developer documentation for Google-related projects. The IBM Style Guide: Conventions for Writers and Editors , 2011, [ 18 ] and Developing Quality Technical Information: A Handbook for Writers and Editors ...
Good documentation is useful in helping people to understand how the software is built and how to use it, but the main point of development is to create software, not documentation. A contract is important but is not a substitute for working closely with customers to discover what they need.
GxP is a general abbreviation for the "good practice" quality guidelines and regulations. The "x" stands for the various fields, including the pharmaceutical and food industries, for example good agricultural practice, or GAP.
Most email software and applications have an account settings menu where you'll need to update the IMAP or POP3 settings. When entering your account info, make sure you use your full email address, including @aol.com, and that the SSL encryption is enabled for incoming and outgoing mail.
Good pharmacovigilance practice (GVP), for the safety of produced drugs; Good regulatory practice (GRP), for the management of regulatory commitments, procedures and documentation; Collectively, these and other good-practice requirements are referred to as "GxP" requirements, all of which follow similar philosophies. Other examples include good ...