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Regulatory document management

Control your content  

​​​​​Managing regulatory documents in life sciences is a time-consuming and costly endeavor due to regulatory requirements and GxP validation. That is why more and more companies are adopting enterprise content management systems to gain a unified view of all content from the point of creation to submission to the authorities. 
 
NNIT has extensive experience designing, developing, implementing, supporting and hosting GxP validated enterprise content management systems that support the entire submission process. We work with leading systems, including CSC FirstDoc, Veeva Vault and EMC D2.
 
Given our experience, we can confidently guide you through the different processes and systems, and design a solution that increases compliance, improves data transparency and reusability, while reducing manual processes – a solution that will match your business challenges.

 

 

 

Niels Buch Leander +45 3075 5339nbln@nnit.comManaging Consultanthttps://www.linkedin.com/in/nielsbuchleanderNiels Buch Leander

 

 

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