Specialized Translation Services
Biomedical translation requires precision and up-to-date technical knowledge from the translators. It also requires multiple levels of quality control and understanding of stringent regulatory requirements, especially in the US, European Union, and Japan.

Whether translating patient case report forms for FDA submission, or packaging for in-vitro devices to comply with EU's IVDD directive, there can be no compromise when boundaries of language and healthcare regulation are crossed.

Pharmaceutical companies, clinical research organizations (CROs), manufacturers of medical and surgical devices, biotech companies, as well as health care managers have come to rely on DeJump's unique methodology when they need clear, correct, and consistent translation of the high-risk, high-value information on which the field of international medicine and biotechnology depends.

We can help you translate or author:
- Case report forms (CRF)
- Clinical protocols
- Clinical trials
- Consent forms
- Data sheets
- Dossiers

- Drug registration documentation
- Insert leaflets
- Manuals
- Manufacturing process description
- Package inserts and labels
- Patient Information
- Patient Questionnaires
- Pharmacological studies
- Product Labels
- Regulatory Documents
- Scientific Papers
- Toxicology Reports