Stratos Recommended for ISO 13485 Certification

 
SEATTLE - Oct. 29, 2015 - PRLog -- Stratos Product Development (http://www.stratos.com/) announced today that it has been recommended for certification to ISO 13485:2003, the internationally recognized quality standard for medical devices.

The recommendation is a result of an extensive assessment performed by BSI Group, and indicates that Stratos’ Quality Management System has been effectively implemented to the requirements of ISO 13485.

As the medical device industry faces intensifying regulatory scrutiny over supplier qualification and control, manufacturers are increasingly motivated to engage development partners who are certified by recognized standards.  Stratos’ proven track record of delivering safe and effective medical device designs to our clients is further bolstered by the achievement of this milestone.

“Our team consistently implements efficient, ISO 13485 design controls and delivers high-value product solutions to our clients,” said CEO Allan Stephan. “This recommendation for certification is a great confirmation of that and will help us bring even more value to our clients.”

Certification is anticipated to be finalized in the next month.

About Stratos Product Development

Since 1987, Stratos has been the trusted resource for science and technology innovators. Whether solving incredibly complex technical challenges, or bringing new market opportunities to fruition, our product designers and engineers can be counted on to deliver. Our collaborative, cross-discipline approach enables us to reduce time-to-market, maximize product opportunities and create compelling product solutions for users and unmet needs in the marketplace. Contact Stratos to take your next product idea from possibility to reality.

Contact
Stratos Product Development
Stephanie Ginger
***@stratos.com
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Tags:Iso 13485, Medical Device Design, Product Development
Industry:Biotech
Location:Seattle - Washington - United States
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