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Global regulatory intelligence at your fingertips

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A single, authoritative source of global regulatory intelligence

IDRAC® from Thomson Scientific brings together everything you need to keep up with the ever-changing regulatory requirements in more than 50 countries and regions, replacing the onerous and time-consuming tasks of acquiring, compiling, indexing, cross-referencing, updating and analyzing this information. Tens of thousands of documents cover all aspects of drug development in each country or region, thematically organized for easy retrieval, with more added every day.

  • Original regulatory and legislative reference texts normally in the local language (with complementary translations into English for China, Japan, Taiwan, Thailand, South Korea and Vietnam)
  • Unique explanatory documents written in English by our team of experts to explain key processes and trends in each country

Every document includes a title, source, abstract, comprehensive and intuitive keywords in English, and rich hyperlinks. A powerful search engine enables you to interrogate the entire database in seconds using full text, title, and keyword searches.

Outstanding flexibility and service

You can build the coverage that suits you by subscribing only to the countries relevant to your organization. As standard, every IDRAC subscription also includes free access to an extensive library of reference texts and explanatory documents covering international organizations such as ICH, WHO, PIC, and many others.

IDRAC is supported by a team of global regulatory affairs professionals and database management and online development experts. Training is provided by qualified instructors who can visit your site at your convenience or host a virtual training session online.

You will also receive comprehensive customer service through easy-to-follow product manuals, dedicated telephone and email helpdesk support and our regular IDRAC newsletter.

 

Receive a quotation or product demonstration

Contact us today for more information click here.


Further information

Click here to download the IDRAC fact sheet

 

 

What you can do
  • Access more than 60,000 essential documents
  • Speed up access to the information you need
  • Track changes to and history of official documents
  • Trace each step of new regulations and directives
  • Navigate easily between documents
  • Receive configurable email alerts
  • Facilitate better collaboration

When you can benefit
  • Registering products and keeping them on market
  • Planning your global registration strategy
  • Preparing for an advisory Committee meeting
  • Preparing to launch an orphan drug, an herbal medical product or generics
  • Planning clinical trials
  • Monitoring the competition

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