Factsheet

Cencora regulatory publishing services

Cencora is a trusted regulatory publishing partner for life science organizations worldwide, providing flexible, scalable end-to-end dossier management across the product life cycle. With 25+ years of regulatory operations experience, we help teams meet evolving health authority requirements while reducing in-house system burden through fully managed technology and global expert hubs covering document formatting, publishing, validation, and submission management.
Cencora Regulatory Publishing PDF image

Download the factsheet to discover:

Cencora Regulatory Publishing PDF image
  • How we help address common challenges of in-house regulatory publishing, including cost, scalability, regulatory change, and QC/validation
  • Details of Cencora’s end-to-end publishing support, from content planning through QC, dispatch, and archiving
  • The regions and submission types supported, including eCTD and portal submissions across key markets
  • How managed services can reduce tool licensing/training/maintenance costs and increase flexibility
Cencora Regulatory Publishing PDF image

Connect with our team

Our team of leading value experts is dedicated to transforming evidence, policy insights, and market intelligence into effective global market access strategies. Let us help you navigate today’s complex healthcare landscape with confidence. Reach out to discover how we can support your goals.

Related resources

Article

Navigating today’s regulatory publishing challenges: How life science companies are adapting

Webinar

Regulatory Data Initiatives in the EU – What you need to know for 2026

Article

Digital twins and hybrid models in biologics production: A model comparison