<img height="1" width="1" style="display:none" src="https://www.facebook.com/tr?id=377593866636424&amp;ev=PageView&amp;noscript=1">

#StayConnected

Regulatory Submissions

Why You Should Select a Regulatory EDMS with RIM Functionality

For pharmaceutical and biotechnology teams, managing documents between program stakeholders is often labour-intensive and disorganized. Information and content tend to be in manual, error-prone Excel tracking sheets or costly, customized legacy systems. As a result, sponsor teams experience significant challenges in managing all the documentation and correspondence associated with global submissions and product registrations.