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About Crimson Life Sciences

Founded in 1992, Crimson is the only translation practice devoted exclusively to Class II and III devices and List A and B IVDs. Crimson is the first translation practice in the world certified to ISO 9001:2008, ISO 13485:2003 and registered to ISO 14971:2007. Crimson has received official Notified Body recognition for its innovative application of the SAE J2450 translation quality standard. The company's specialized approach to translation risk management is the basis of the industry's only risk management patent (pending).

Crimson's specialized approach to medical technology translation has been featured in industry publications such as Medical Device & Diagnostics Industry, BI&T Journal (AAMI publication), Orthopedic Design & Technology, and Medical Products Outsourcing.

In 2005, Crimson joined the growing TransPerfect family of companies. Clients benefit from Crimson's audited quality and risk management systems, combined with the extensive technology resources and localization talent of TransPerfect and its software localization unit, Translations.com.

 


Expert Opinion Forum
06/16/2010
Reimbursement Opportunities for Medical Device Manufacturers
11/03/2009
MDD Revision: Are gas pathways subject to the phthalate regulation?
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Bulletins
07/06/2009
New Disclosure Laws for Medical Device Companies
06/09/2009
Crimson Introduces "Expert Opinion" Webinar Series
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Publications
09/01/2009
Growing Regulatory Concern for Outsourcing
05/01/2009
Getting More for Less: The Alchemy of Risk Management
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Industry News
06/17/2010
India to Begin Regulating All Medical Devices
04/20/2010
"Explosion" of Home Health Devices Fuels FDA Oversight
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