Life Sciences
Precision is everything.
In the life science arena, accuracy in translation
is absolutely crucial.
Communicating effectively in other languages is not only a
matter of strengthening your business' competitive health—it could
also impact your customers' health.
Maximizing global life science opportunities in diverse markets
and regulatory environments requires expert multilingual communications
solutions.
European Commission Regulations
As of December 7, 2003, all medical devices and in vitro
diagnostics equipment on the European market must carry the “CE”
mark denoting compliance with all European Commission regulations.
These newly-enacted regulations include important translation
requirements to ensure the safe use of devices throughout the
European market. Due to the multitude of languages used within the
area, the European Commission requires manufacturers to meet the
language requirements of each individual member state in which their
products will be sold, in order to obtain “CE marking.” At this
point, any device placed on the market must be CE-marked. After
December 7, 2005, the regulations become even more stringent: a CE
mark is required on any device being put into service in the
European Economic Area.
Auracom International can help!
Our communications professionals speak the languages of your markets
and the language of the life science industry.
It's a powerful combination.
We deliver world-class translation and multilingual communication
solutions for the full spectrum of medical and pharmaceutical communications
needs, including:
- Biotechnology
- Case Report Forms (CRF)
- Clinical Protocols
- Clinical
Trials
- Drug Registration Documentation
- In Vitro Diagnostic Devices (IVDD)
- Manuals
- Manufacturing Process Description
- Medical Devices
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- Medical Information Technology
- Medical Software
-
Monograms
- Package Inserts and Labels
- Pharmaceutical
- Pharmacological Studies
- Regulatory Documents
- Scientific Papers
- Technical Documentation
- Toxicology Reports
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