Proposal development

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Most of the common tools for publishing help material fall short when it comes to API documentation. Much API documentation (such as for Java, C++, or .NET APIs) is generated from comments in the source code. Their outputs don’t usually integrate with other help material, such as programming tutorials or scenario-based code samples. REST APIs are a breed of their own, with almost no standard tools for generating documentation from the source. The variety of outputs for REST APIs are as diverse as the APIs themselves, as you can see by browsing the 11,000+ web APIs on programmableweb.com. As a technical writer, what publishing strategies do you use for API documentation? Do you leave the reference material separate from the tutorials and code samples? Do you convert everything to DITA and merge it into a single output? Do you build your own help system from scratch that imports your REST API information? There’s not a one-size-fits-all approach. In this presentation, you’ll learn a variety of publishing strategies for different kinds of APIs, with examples of what works well for developer audiences. No matter what kind of API you’re working with, you’ll benefit from this survey of the API doc publishing scene. - See more at: http://idratherbewriting.com

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Many sponsors are concerned with the risks and costs involved in ensuring that their electronic systems comply with the FDA’s ruling on acceptance of Electronic Records and Electronic Signatures in place of their paper equivalents (21 CFR Part 11). Although the ruling has been in place since 1997, there is often a lack of clarity concerning what characteristics and features a software solution must have to comply with 21 CFR Part 11. Even when a solution meets all of its requirements, ensuring that procedural requirements are met may be a bigger challenge. Although sponsors’ concerns are certainly valid, Part 11 compliance also provides an opportunity. Sponsors and the FDA share a common goal of ensuring the integrity of their data, documentation and computer systems. If Part 11 compliance can be achieved by software configured to represent the sponsor’s desired business process, the burden on both system users and IT administrators can be minimal. The sponsor can then achieve benefits around both process automation and process transparency. The intent of this paper is to describe how NextDocs products provide a built-in platform for 21 CFR Part 11 compliance while providing capabilities that allow sponsors to automate, monitor and control their processes.

21 CFR Part 11 Challenges and Solutions - White Paper

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Proposal development

1. Proposal development