Reduce administration and maintain compliance
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Clinical, regulatory, and commercial teams have saved over 90% of the time previously spent managing translation processes.
Streamline and simplify multilingual pharmaceutical documentation management with a Veeva-certified integration into GlobalLink, the industry’s leading translation management system.
Check out our checklist for reducing complexity, costs, and turnaround times.
See how we helped leading sponsors like Sanofi centralize their clinical translation process.
Reduce project management time and project timelines by more than 90%
Reduce administration and maintain compliance
Mitigate risk with GXP, GMP, and CFR Part 11-compliant technology
Ensure consistency while reducing costs and turnaround times
Drive transparency, control, and continuous improvement with advanced reporting
A checklist for reducing complexity, costs, and turnaround times.
Increased pressure to expedite clinical research startup timelines.
Reduced budgets and increased pressure to manage costs.
An ever-evolving global regulatory landscape.
| Activity |
Without Integration |
With Integration |
Time Reduction |
|---|---|---|---|
|
Export Content for Translation |
30 Mins |
0 Mins |
100% |
|
Managing Translation Process |
2 Hours |
5 Mins |
96% |
|
In-Country Translation & Review Updates |
3 Hours |
30 Mins |
83% |
|
Import to Veeva |
30 Mins |
0 Mins |
100% |
Veeva Partner
since 2019
Future Veeva Vault
upgrades included
Customizable reporting
and audit trails
Compatible with any
Veeva Vault product
5000+ clients
running GlobalLink
Translation vendor-
agnostic
Compatible with Veeva
Vault object fields and
library documents
Validated & 21 CFR
Part 11 compliant
200+ full-time
GlobalLink developers
& support staff
Pharma-specific
AI translation models
