Clinical Trial Management
Clinical trials often need to be carried out in multiple countries and regions. Having a technologically advanced and experienced translation partner is essential for efficient communication between researchers and patients, and also benefits patients across the world by speeding up the output of new treatments.
Our services
The translation of clinical trial documents is often urgent and delivery times are often not fixed. We have extensive experience with multilingual clinical trial documents, and can provide appropriate translation for various documents, including:Clinical trial protocols and revisions
Researcher manuals
Case report forms (CRFs)
Informed consent forms/HIPAA/Consent forms
Clinical outcome assessment questionnaires (COAs/PROs)
Contracts
eCOA/ePROs
Ethics Committee review applications
Patient safety cards
Patient questionnaires
Patient journals / incident reports
Patient records
Protocols
Protocol summaries
Adverse event reports
Other clinical documents
How we help you succeed
Throughout the many stages of clinical trials, there are different translation requirements for the evaluation of drug safety and effectiveness, drug use specifications and patient records.We have standardized procedures for each different category of clinical trial translation. From translation and proofreading by industry experts, to additional quality control, emergency services work, multilingual audio-visual content, notarization and certification and many more, we can help. We can also customize our approach to deliver content that meets any special requirement you may have.Contact Us
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