YOU'LL BE ABLE TO

Utilize efficient and compliant change control tracking of product detail, data and submission documents

  • Access a regulatory focused data library and reporting framework
  • Locate publishing support for eCTD, paper, hybrid, NeEs, medical device (PMA/510k), and others
  • More effectively manage the entire regulatory information lifecycle






 

LIQUENT Regulatory Software and Related Services

LIQUENT SOFTWARE AND SERVICE OFFERINGS ENSURE CLIENTS MEET THE STRICT STANDARDS ENFORCED BY REGULATORY AUTHORITIES ACROSS THE WORLD.

BY PROVIDING ACCESS TO OUR PROVEN EXPERTISE WITHIN THE MARKET, OUR CONSULTING TEAM WORKS DIRECTLY WITH OUR OTHER ORAGANIZATIONS TO HELP GUIDE YOU THROUGH YOUR ENTIRE LIFECYCLE.

As industry and regulatory authorities look to unify the submission structures through the CTD and eCTD, Life Sciences organizations are looking for integrated solutions that can effectively manage product registrations, dossiers and documents over time.

LIQUENT InSight is the first and only product suite to provide a centralized, global view of product details, documents, and submissions to support collaboration, compliance requirements and the eCTD.

  • Submission materials via product and application information
  • The ability to effectively manage the entire regulatory information lifecycle
  • Internal resources to focus on core competencies
  • Traditional paper CTDs and hybrids
  • Over 300 paper CTDs in the US

If you would like additional information please contact us.