IDRAC®, the complete pharmaceutical regulatory intelligence solution from Thomson Reuters, equips your organization to stay fully up to date with the ever-changing requirements of governments and regulatory authorities around the world. Only IDRAC has the global reach, depth of analysis and local expert knowledge to keep you informed of every regulation that could affect your product.

Reference Documents – Regulatory Summaries – Regulatory Intelligence Reports – Global Module
The IDRAC database not only provides you with the most complete daily updated and historical repository of Reference Documents. It provides you with continuously updated Regulatory Summaries, entirely in English, that are written by our team of regulatory experts with input from our network of local regulatory consultants. IDRAC also provides you with Regulatory Intelligence Reports that are essential tools to support your activity and save you time in analyzing the Regulatory Information. The Global Module is an access point for users who work with more than one IDRAC country module. It provides content, regulatory expertise and visual enhancements to aid comparisons between the regulatory requirements in multiple countries and regions.

This is why IDRAC is the solution the world’s most demanding pharmaceutical companies rely on to guide their regulatory decisions, day after day.