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MasterControl Provides 2016 Compliance Guidance at Medical Design & Manufacturing (MD&M) West 2016 Show - MasterControl will offer valuable resources at this year’s MD&M West Expo for what the medical device industry should address in 2016 for ISO 13485:2016 and process validation - MasterControl.com
MasterControl Provides 2016 Compliance Guidance at Medical Design & Manufacturing (MD&M) West 2016 Show

 

NewswireToday - /newswire/ - Salt Lake City, UT, United States, 2016/02/05 - MasterControl will offer valuable resources at this year’s MD&M West Expo for what the medical device industry should address in 2016 for ISO 13485:2016 and process validation - MasterControl.com.

   
 
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MasterControl (MD&M West booth #2844), a leading global provider of electronic quality management systems (EQMS) and quality consulting services, will offer valuable resources at this year’s MD&M West Expo for what the medical device industry should address in 2016 for ISO 13485:2016 and process validation.

For MD&M West, the largest medical manufacturing event in the world running February 9-11 in Anaheim, California, MasterControl will be launching the first of a three-part video series on ISO 13485:2016. ISO 13485:2016 Part 1: Getting Ready for Changes will cover an overview of what, why, when and how ISO 13485:2003 is changing this year.

At MD&M West, on February 11, Walt Murray, Director of Quality & Compliance Services, for MasterControl, will be speaking as part of the show’s focus on enhanced quality assurance and risk management. At 11:00 am. - 11:45 am. Mr. Murray will cover “Process Validation Planning: Have You Made the Leap into the 21st Century?” This presentation will provide useful information regarding the FDA's Center for Devices and Radiological Health (CDRH) recent posting “CDRH Fiscal Year 2016 Proposed Guidance Development and Focused Retrospective Review of Final Guidance.’”

About MasterControl

MasterControl, Inc. (mastercontrol.com) is a committed team of quality, regulatory and software experts who work to empower regulated companies to get their products to market faster. MasterControl's quality management software solutions reduce overall costs, increase efficiency and accelerate compliance, creating a significant competitive advantage for customers. Drawing upon unparalleled industry experience, MasterControl offers a suite of seamlessly integrated and scalable software solutions for quality management, document control, product lifecycle management, supplier management, audit management, training management and much more. MasterControl's complete quality management solution is designed for easy implementation, validation and use, continually improving on the promise of Compliance Accelerated.

For more information about MasterControl, call 1.800.825.9117 (U.S.); +44 (0) 1256 325 949 (Europe); +81 (03) 5422 6665 (Japan); or +61 (3) 9717 9727 (Australia).

 
 
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Written by / Agency / Source: MasterControl, Inc.

 
 

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MasterControl Provides 2016 Compliance Guidance at Medical Design & Manufacturing (MD&M) West 2016 Show

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