Specialist areas
In our work, we bear in mind that in medical technology the latest state of medical research and the resultant knowledge about more effective, patient-friendlier and cheaper methods of treatment are combined with technical innovations and currently available technologies.
In the medical technology field, we cover the whole gamut of documentation for instruments, apparatuses and systems, both in the area of manufacture and in that of testing and operation.
In vitro diagnostics
Similarly, in the extensive field of IVDs, whether reagents, calibration material, kits or apparatuses, the latest medical and natural science findings in the fields of medicine, biochemistry, molecular biology and chemistry are combined with the latest technological possibilities of early and reliable diagnosis.
Our laboratory clinicians, biochemists and technicians are acquainted with these latest procedures and the corresponding documentation of IVDs.
Both medical technology products and in vitro diagnostics must be manufactured according to European guidelines under a quality assurance system. For this, appropriate technical documentation must be available.
We relieve you of all the translation processes that occur in your product cycle up to the technical documentation of your medical technology product or in vitro diagnostic device.
We translate
- Instructions for use
- Patient instructions and leaflets
- Apparatus descriptions
- Data sheets
- Applied technical standards
- CE certificates
- Business reports
- Clinical trials
- CoC = Certificate of Conformity
- QM documentation
- Construction plans and calculations, manufacturing procedures, technical tests
- Medical and expert reports
- Presentations
- Product monographs
- Publications (e.g. advertising brochures, journals, …)
- QM systems and certificate
- Documentation and explanations of products for in-house training
- Training modules
- Safety specifications
- Software
- Technical documentation
- Video scripts, film scripts
- Websites