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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.
Download the factsheet to discover:
- 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
Neem contact op met ons team
Ons ervaren team van waarde-experts creëert op basis van bewijsmateriaal, beleidsinzichten en marktinformatie effectieve strategieën voor toegang tot wereldwijde markten. We maken u wegwijs in de complexe wereld van de gezondheidszorg in verschillende delen van de wereld. Neem contact op om te ontdekken hoe we uw doelen kunnen ondersteunen.
