Thomson Reuters

"I need to take the uncertainty out of my regulatory obligations."

 

Overview

By the time it comes to the last hurdle, there shouldn’t still be any risk involved.

You’ve been developing the product for long enough — you should expect to move swiftly and easily through the regulatory and market approval processes and reimbursement negotiations. So why do you still have sleepless nights?

Thomson Reuters can equip you with the expert guidance, tools and technology you need to smooth your passage to approval. We can draw on the industry’s leading regulatory intelligence database to provide your organization with unparalleled regulatory and submission experience.

Our experts can advise you how to approach new and emerging markets, all over the world. As more stringent regulations come in, we’ll keep you fully informed.

We can define, manage and implement your entire submission process, reducing the risk of missed deadlines and cost overruns. We’ll show you how to increase teamwork, reuse planning for each successive project, and realize your departmental efficiencies.

Then, when you’ve achieved launch, we’ll help you comply fully with your pharmacovigilance responsibilities.

More information on Regulatory Software, Benchmarking and Regulatory & Clinical Services...

Intelligence

LEADING REGULATORY INTELLIGENCE SOLUTIONS

• IDRAC®: A competitive edge in regulatory intelligence. A single, authoritative source of global regulatory requirements
• IDRAC® Regulatory Online Learning: Expert pharmaceutical industry training from Thomson Reuters
• Thomson Pharma®:  Comprehensive global pharmaceutical information solution
• Prous Science Integrity®:  Integrated drug discovery and development portal

Technology

UNPARALLELED REGULATORY SUBMISSION EXPERIENCE

• Liquent InSight : A centralized, global view of regulatory documents and submissions software
• Liquent Regulatory Software Consulting: Aids organizations in all aspects of the submission process
• Liquent Regulatory Software and Related Training: Offering on-site, public, private, and customized training programs
• Liquent Regulatory Strategies: Helps identify what you need to be successful, ensuring a smoother process from start to finish

Regulatory Service

DEFINE, MANAGE AND IMPLEMENT YOUR ENTIRE REGULATORY PROJECTS 

• eCTD creation and lifecycle management
• Onsite submission support
• Medical communications
• Report publishing, scanning and printing services
• Regulatory or medical writing needs
• Frequent updates on new drugs, trials, stories and patent
• Developing regulatory strategies
• Identifying submission options
• Custom Information Services
• Many more regulatory-related duties