Clinical Trial Translation

From pre-clinical to post-launch, we take your product to the global marketplace to improve lives

We understand your clinical trial documents need more than rigorous quality control and accuracy. There is no room for delays and errors that affect data collection.

At G3 Life Sciences, we have perfected our workflow to match your needs and ensure our linguists have the required certifications and adhere to regulatory and good clinical practice (GCP) guidelines.

We can handle all types of documents, including:

ICFs
eCOAs
Questionnaires
Patient Surveys
PROs
COAs
Adverse Events
Patient Diaries
Study Protocols
Medical Safety Reports
CRFs

Expert Linguist Network

Network of over 4,000 certified linguists with subject-matter expertise

Diversity & Inclusion

Committed to applying our services to promote diversity & inclusion and achieve health equity

Certifications

ISO 17100, ISO 18587, ISO 9001, and WBENC certified

Other Services:

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