is being presented by Andres Heuberger, President, of ForeignExchange Translations, Inc. and airs on Wednesday, August 31st, 2011. For more details on this event or to register, please visit our site at www.fxconferences.com
It's challenging enough for manufacturers to deal with evolving EU regulations, never mind that your head is spinning from coordinating the reviews of multiple translated components in numerous countries!
Internal politics, miscommunication across time zones, and vacation schedules can make translation reviews an expensive and time-consuming process. Rather than shifting responsibility overseas or skipping reviews altogether, attend this advanced audio conference.
With proper planning, open communication, and strong vendor relationships, it is possible to reduce turnaround time, keep translation costs manageable and even avoid a few headaches. This presentation shows you how.
Over 50,000 attendees across hundreds of companies have taken advantage of our easy-to-use audio conferences to stay abreast of a fast-changing business environment. We specialize in Life Science conferences, along with topics relevant for HR, Marketing, Legal, and Finance professionals. Come check out our library of past audio conferences and see what's upcoming at FXConferences
Showing posts with label in-country review. Show all posts
Showing posts with label in-country review. Show all posts
Tuesday, August 9, 2011
Monday, May 17, 2010
Best Practices for Managing In-Country Translation Reviews
is being presented by Andres Heuberger, President, of ForeignExchange Translations, and airs on Thursday, June 24th, 2010. For more details or to register, please visit our site at www.fxconferences.com
It's challenging enough for manufacturers to deal with evolving EU regulations, never mind that your head is spinning from coordinating the reviews of multiple translated components in numerous countries!
Internal politics, miscommunication across time zones, and vacation schedules can make translation reviews an expensive and time-consuming process. Rather than shifting responsibility overseas or skipping reviews altogether, attend this advanced audio conference.
With proper planning, open communication, and strong vendor relationships, it is possible to reduce turnaround time, keep translation costs manageable and even avoid a few headaches. This presentation shows you how.
It's challenging enough for manufacturers to deal with evolving EU regulations, never mind that your head is spinning from coordinating the reviews of multiple translated components in numerous countries!
Internal politics, miscommunication across time zones, and vacation schedules can make translation reviews an expensive and time-consuming process. Rather than shifting responsibility overseas or skipping reviews altogether, attend this advanced audio conference.
With proper planning, open communication, and strong vendor relationships, it is possible to reduce turnaround time, keep translation costs manageable and even avoid a few headaches. This presentation shows you how.
Thursday, August 6, 2009
CE Marking: Pitfalls and Best Practices for IVD Directive Language Requirements
The $9 billion U.S. in vitro diagnostics (IVD) industry is ill prepared to meet the strict new regulations contained in the European Union's new IVD Directive. With only four business quarters left before the December 2003 deadline, IVD companies are realizing that translation is critical to earning the CE mark.
Manufacturers that lack effective plans for complying with the language requirements of the directive risk losing revenue and market share. Translation quality control, global labeling strategies and in-country reviews present new challenges for the majority of diagnostics manufacturers who are dealing with non-English texts for the first time.
CE Marking: Pitfalls and Best Practices for IVD Directive Language Requirements was presented by Andres Heuberger, President, with ForeignExchange Translations, Inc. and was previously recorded. For more details, or to download this conference please visit our site at www.fxconferences.com
Manufacturers that lack effective plans for complying with the language requirements of the directive risk losing revenue and market share. Translation quality control, global labeling strategies and in-country reviews present new challenges for the majority of diagnostics manufacturers who are dealing with non-English texts for the first time.
CE Marking: Pitfalls and Best Practices for IVD Directive Language Requirements was presented by Andres Heuberger, President, with ForeignExchange Translations, Inc. and was previously recorded. For more details, or to download this conference please visit our site at www.fxconferences.com
Subscribe to:
Posts (Atom)