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ReALM® Regulatory Intelligence module allows for the management of curated regulatory requirements (both hard and soft intelligence) in actionable ways through a master library of global requirements. The library is made available in checklist format for various regulatory and submission activities. Regulatory intelligence includes a layered approach including collection and management of policies, regulations, guidelines, subject matter interpretations, best practices, and company experiences or prior knowledge. 

Regulatory requirements can be applied to create checklists for specific products and activities, for example, preparing a clinical trial application or creating an NDA submission for a specific country. These predefined checklists are based on health authority requirements and can be further modified by a regulatory strategist for specific products based on product strategy and negotiations with respective health authorities.

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