SPEED UP REGULATORY APPROVALS WITH MULTILINGUAL
IMP LABELING SERVICES.
Automate. Simplify. Speed Up.
TransPerfect Life Sciences’ helps clinical supply labeling teams meet regulatory compliance quickly and efficiently.
Our resources are readily available to scale and complete regulatory reviews and translations for any country or any label type using our ISO-certified process and 21 CFR Part 11-compliant technology.
With a 98.5% first-time approval rate, we are the proud preferred partner of leading clinical supply teams such as Eli Lilly, AstraZeneca, PCI, and more.
___________
___________
Centralized labeling workflow management
Streamline workflows and processes with our 21 CFR Part 11 compliant and validated technology that unifies all project management needs—including project submission, quoting, tracking, and delivery.
Reliable support you can trust
We specialize in overseeing clinical label project review and coordination with our network of regulatory experts, linguistic teams, and internal regulatory resources.
Quality-first mentality
Our team of regulatory experts and certified linguists take the time to understand your QA processes to meet your expectations and requirements.
Flexibility and agility to meet your unique needs
For every partner we work with, we maintain flexibility and agility to adapt to their current processes and, as needed, provide industry-standard workflows.
DISCOVER OUR END-TO-END IMP LABELING PROCESS
Creation & Translation
of Labels
Custom Technology
Integrations
ISO-Certified Linguist
& Translation Process
Translation Management
for Automation Capabiltiies
Industry Resources &
In-House Expertise
Consultation & Review
of Regulatory Labels
WE'VE HELPED CLINICAL SUPPLY TEAMS ACHIEVE
50%
Faster timelines
25%
Reduction in project management hours
100%
Compliance
