ACUTA Regulatory Intelligent Documents (ARID)

ACUTA LLC

ACUTA Regulatory Intelligent Documents (ARID)

Document Authoring Processes.

Clinical Administration And Documentation Clinical Documentation

Do you know anyone using ACUTA Regulatory Intelligent Documents (ARID)?

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.

ACUTA Regulatory Intelligent Documents (ARID)