Bringing a drug to market means complying with complex regulations in a highly competitive environment where cost control is crucial. Translation is required at many stages of the product cycle, including clinical research, regulatory submissions, manufacturing, marketing and packaging.
Our team understands that you need precise, timely and compliant translations and will support you throughout your product life cycle with customised, high-quality multilingual solutions.
Translation services for pharmaceutical documents
The typical documents we translate for our pharmaceutical industry clients include:
- Clinical protocols
- Data sheets
- Investigator brochures
- Informed consent forms (ICFs)
- Package and labelling
- Patient information
- Pharmacological studies
- Regulatory documents
- Summaries of product characteristics (SPCs)
- Patient information leaflets (PILs)
- Toxicology reports
- Marketing communication texts