Today, regulatory challenges, user acceptance and risk management are as important as your products’ underlying technology.
From clinical trial results to consumer product labeling, you can be confident that ULG-translated documentation conforms to all global requirements. We understand scientific language and processes, as well as the context in which documentation may be used. Plus, we customize our approach by testing and adapting quality procedures that respond to the unique and ever-changing life-sciences regulatory environment.
Our ISO-certified processes help you manage risk in a complex and highly-regulated environment. With ULG, you can be confident in receiving sound risk-management advice during global expansion, as well as expert consulting on localization and regulatory compliance trends.
View our specialized translation + interpreting services for life sciences.
Protocols & protocol synopsis
Ethics committee letters
Packaging and labeling material including SPL environments
SmPCs Product Labels Package Inserts CTDs
eCTDs Protocols PILs
Websites Press Releases Presentations
Brochures Executive Speeches Newsletters
Adverse Event Report Forms Death Certificates
CIOMS Aggregate Reports
Datasheets Certificates of Analysis SOPs
Validation Documentation Batch Manufacturing Records IFUs/DFUs
Clinical Trial Contracts Insurance Policies & Certificates Employment Contracts
Trademark Documents Patents
Patent Disputes Government Decrees
PIM Training Manuals
eLearning User Manuals
Over-the-Phone Interpretation (OPI) In-Person Interpretation Video Remote Interpretation (VRI) Conference + Meeting Interpretation
“ULG feels like another department within our company. Their integration with our international, technical and marketing teams and their adaptation to our company culture has allowed us to compete within the global market.”
– Labeling manager, Medtronic
Driven by quality,
powered by experience.
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5 Reasons Why Latin America is Great for Conducting Clinical Trials
New EU Medical Device Regulations Take Effect: A Summary of the MDR and IVDR
Leveraging Translation Memories In Clinical Trial Translations