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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.