Document Expertise

When you choose Corporate Translations, you receive a level of service that can come only from a provider who knows the pharmaceutical, biotech, and medical device industries. Our proven methodology, specialized translation professionals, and expertise in the life science industry makes us well qualified to translate and desktop publish documents through all phases of drug development. From CRFs to patient diaries and PRO instruments, we ensure that every job is performed with speed and precision.

  • Biological screening
  • Expert reports
  • Journal articles
  • Synthesis and extraction
  • Pharmaceutical dosage formulation
  • Pharmacological testing
  • Stability testing
  • Toxicology and safety testing
  • Adverse event reports
  • Bioavailability studies
  • Case Report Forms
  • Case Report Forms – executed with handwritten comments
  • Informed consents
  • Investigator CVs
  • Palm-based software libraries
  • Patient diaries
  • Patient Reported Outcomes
  • ePROs
  • Phase I, II, and III clinical evaluations
  • Surveys
  • Complaint lines
  • Investigational New Drug (IND) Application
  • New Drug Application (NDA)
  • Packaging
  • Post-approval research
  • Prescribing information
  • Protocols
  • Batch records
  • Patents
  • Process development
  • Quality control
  • Advertising
  • Brochures
  • Press releases
  • Websites
  • Audio/videotapes, DVDs
  • Employee satisfaction surveys
  • Code of conduct policies
  • Training manuals
  • Video role play
  • Job listings
  • SOPs
  • Company newsletters