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@ShahidNShah
@ShahidNShah
Document Authoring Processes.
Clinical Administration And Documentation Clinical Documentation
ACUTA Regulatory Intelligent Documents (ARID) is a set of over 250 shell documents defined by regulatory agencies and the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), covering the marketing and clinical trial application processes for Europe, the United States, and Canada.
A compact, focused version of the Microsoft Office Word toolbars, and a menu-driven system to select from agency-specified shell documents for submissions give ARID users a quick start on regulatory authoring. ARID’s function to create a New Document guides you through selection of the right shell document for the work you need to do, drilling down through the specific region and module to the particular document type for the task.
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