Specifically, submitted PDF files must be compatible with Acrobat 8.0, without requiring additional software like plug-ins. PDF VersionįDA Guidelines: The FDA accepts PDF versions 1.4 to 1.7. In the following sections, I have outlined each of the key areas mentioned, common areas of difficulty, along with the relevant functionality of Aerialist Pharma and Acrobat. Given the importance and stringency of the regulations, this document is surprisingly succinct, clear and simple. There will always be a link to the most recent version of the guidelines here, but as of today, the current guidelines are here (in PDF, of course). That is a fair enough question, I think, and this post is my answer to you. Since then, a lot of you have quite reasonably asked how Aerialist Pharma and Acrobat align with the US FDA regulations themselves, rather than with other products seeking to solve the same problems. A while back, I wrote a blog post comparing TRS ToolBox with the dynamic duo of Aerialist Pharma and Acrobat for preparing regulatory submissions.
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