Medical Translation Services
Clinical trials have become more multinational in scope—and more complex. More than ever, patient data requires the ultimate in control and rigorous process. Exact documentation is paramount. That’s where it’s vital to have a partner like OmniLingua Worldwide to help you manage risk and ensure patient safety and privacy through high quality clinical trial translation.
OmniLingua has more than 20 years’ experience with medical device and pharmaceutical trial translation. Major Clinical Research Organizations (CROs) view OmniLingua as a reliable, quality-driven supplier. Read our case study to see how OmniLingua has enabled our clients to seamlessly manage large-scale, multinational clinical trials.
We translate to and from all global business languages, using a worldwide network of industry-specific translators with proven translation expertise. We support all clinical trial document translation, including:
- Case Report Forms
- Clinical Protocols
- Clinical Trial Submissions
- Drug Study Labels
- Informed Consent Forms (ICF)
- Patient Information Sheets
- Patient Recorded Outcome (PRO) forms
We also offer full back translation support.
Our documentation process requires:
Compliance to all relevant local and global standards
Strong internal HIPAA and 21 CFR Part 11 document and data control
Processes that are documented and hardwired
Quick execution—which means we’ll help you meet your tight timelines
OmniLingua delivers on quality as evidenced by: