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Industry experts declare that every medical device is defined by a unique combination of product and intended use...
Crimson Life Sciences now provides advanced technology solutions, combined with innovative regulatory strategies, that enable...
   
Safety and effectiveness are guiding principles for the medical device industry. In response, risk management practices have extended...
Crimson provides custom processes that are designed to reduce cost and risk for some of the world’s largest medical device manufacturers...
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 organization in the world certified to ISO 9001:2008, ISO 13485:2003 and registered to ISO 14971:2009. 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).

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Your trusted source for medical device translation, labeling, and industry news
06/01/2010 | Crimson Registers Translation Industry First
05/03/2010 | Avoiding Chinese "Urine Districts"
04/05/2010 | Beware Invented Standards
03/17/2010 | Labeling Errors: Leading Source of Device Recalls
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Crimson provides clients and prospective clients with a variety of valuable third-party research and offers.
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Crimson provides clients and prospective clients with a wealth of original and third-party research and information – including our popular Labeling Symbols Library.
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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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