Science

Regulatory and Clinical Services

eCTD. IND. NDA. MAA. CTA. How do you keep it all straight?

We’ll provide submission outsourcing so your organization doesn’t waste time navigating the complex submission process.

Whether it’s global application filings, content development, customized information services, or submission lifecycle management, the global industry experts at Thomson Reuters will identify, define and standardize your processes, ensuring all your timelines and expectations are met.

And with our full-service suite, you’ll be amazed at the hours you save. We’ll take care of all the most time-consuming tasks, everything from scanning and printing to complex regulatory writing, submission publishing, and lifecycle management.

Our Services Include:

  • 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