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.
Ectd
By
Katherine Cianciarelli |
Feb 21, 2019 10:14:54 AM |
Categories:
Regulatory,
Technology Strategy,
Regulatory Submissions,
eCTD
|
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