Solutions / Regulatory Requirements

Need assistance in obtaining the CE Mark designation? Considering entering the expanded countries of the EU, such as the Czech Republic, Hungary, or Lithuania? Did you know that there are new labeling requirements for Medical Devices in Japan that went into effect on April 1, 2005? Need manuals, and labels translated and typeset in more than 30 languages simultaneously? Need help in setting up and managing an effective In-Country Review (ICR) process? Need a Certificate of Conformity for your translations? Since 1996, we have been helping companies in regulated industries overcome these challenges.