Pharmaceutical & Clinical Research Translation
High quality translations for pharma companies, CROs and regulatory submissions.
We help pharmaceutical companies and clinical research organisations manage multilingual documentation across the product life cycle.
Pharmaceutical translation covers early research, clinical development, regulatory submissions and post marketing safety communication. Accuracy and consistency are critical because translated content is reviewed by regulators, ethics committees, investigators and patients. Our teams work on clinical trial documentation, patient facing materials, regulatory dossiers, pharmacovigilance reports, SmPCs and PILs. We align with terminology used by EMA, FDA and other agencies where relevant and follow your internal style and template frameworks. Whether you run global trials or manage mature products in multiple markets, we help you maintain reliable multilingual documentation and reduce risk of misinterpretation.
Pharmaceutical.
- Clinical trial protocols and IBs
- Informed consent forms and patient diaries
- Regulatory submissions and variation documents
- SmPCs, PILs and labelling content
- Pharmacovigilance and safety reports
- Medical information and HCP communication
Pharmaceutical
- Translating research-heavy scientific documents.
- Ensuring full regulatory compliance in multiple regions.
- Managing terminology across clinical, marketing and regulatory teams.
- Maintaining accuracy in dosage, warnings and studies.
Pharmaceutical
Pharmaceutical?
Pharmaceutical.
Pharmaceutical.
-
Multi country oncology study -
Product information localisation