SERVICES

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In the following subject areas:

Pharmaceuticals

Clinical Trials

Medical Devices

Pharmacovigilance

Regulatory Documents

Medical Journals

Examples of such documentation include:

  • Case reports
  • Clinical Trial Protocols
  • Ethics Committee and Institutional Review Board (IRB) correspondence
  • Informed Consent Forms (ICFs)
  • Investigational Medicinal Product Dossiers (IMPDs)
  • Investigator’s Brochures (IBs)
  • Journal articles
  • Package Inserts
  • Patient Information Leaflets (PILs)
  • Pharmacovigilance/Serious Adverse Event (SAE) reports
  • Research papers
  • Standard Operating Procedures (SOPs)
  • Substantial modifications
  • Summary of Product Characteristics (SPCs)

Get in Touch

Drop me a line at
info@pharmaco-translation.com
or via the contact form, and I will be pleased to discuss your requirements, whether it be the translation of a single-page document, or a more complex linguistic project.

If you prefer to speak by telephone, please phone me on
+44 (0)151 476 6557 – I look forward to your call.