In July 2013, a new mandatory medical device regulatory system came into effect in Malaysia. Manufacturers of medical devices who are planning to continue or start selling medical products in Malaysia should submit an application for medical device registration before June 30, 2016.
Technical writers and authors produce content for their companies under sever deadlines and often with little regard to the varying needs of other countries. Why take unnecessary risk?
Due to economical constraints and global requirements, more patient recruitment companies managing trials involving participants from a number of foreign countries, requiring data and information to not only be translated correctly but to be medically precise and culturally sensitive.