FDAnews Announces — Medical Device Production Equipment and Process Control Webinar, Nov. 17, 2016

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FDANEWS

Oct 26, 2016, 14:30 ET

Falls Church, VA (PRWEB) October 26, 2016 -- Medical Device Production Equipment and Process Control
**An FDAnews Webinar**
Nov. 17, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://www.fdanews.com/mdproductionequipmentprocesscontrol

One of the most crucial and sometimes overlooked elements of QMS is the installation and maintenance of production equipment.

Get ready to implement the changes ISO 13485:2016 requires of a QMS system. Or create an even more effective system by going beyond the minimum requirements.

Join industry expert, Dan O’Leary on Nov. 17 when he’ll discuss how an effective system for production equipment can improve device manufacturing, support a low cost approach and improve equipment operator safety.

After attending this 90-minute webinar attendees will be able to:

  • Understand the QMS requirements in QSR, ISO 13485:2003, and ISO 13485:2016
  • Learn the OSHA standards for machine guarding and LOTO and why to apply them for both installation and maintenance
  • Understand how to incorporate calibration requirements into production equipment maintenance
  • Identify maintenance strategies and their application including time based, activity based, and reliability centered maintenance
  • Learn how to allocate maintenance activities between the operator and the maintenance crew
  • Understand classical equipment effectiveness metrics

BONUS MATERIALS: Participants will receive an activity analysis based on the three QMS versions and the OSHA regulations.

Register today for a comprehensive assessment of what’s needed for effective implementation.

Meet the Presenter:
Dan O’Leary is the President of Ombu Enterprises, LLC., a company offering training and execution in Operational Excellence, focused on analytic skills; and a systems approach to operations management. Dan has more than 30 years experience in quality, operations and program management in regulated industries including: aviation, defense, medical devices and clinical labs. He has a Masters Degree in Mathematics; is an ASQ certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer and Six Sigma Black Belt; and is certified by APICS in Resource Management.

Who Will Benefit:

  • Production Managers
  • Production Supervisors
  • Manufacturing Engineering Managers
  • Manufacturing Engineers
  • Quality Managers
  • Quality Engineers
  • Reliability Engineers
  • Maintenance Managers
  • Maintenance Supervisors

Webinar Details:
Medical Device Production Equipment and Process Control
**An FDAnews Webinar**
Nov. 17, 2016 — 1:30 p.m. – 3:00 p.m. ET
http://www.fdanews.com/mdproductionequipmentprocesscontrol

Tuition:
$287 per site

Easy Ways to Register:
Online:     http://www.fdanews.com/mdproductionequipmentprocesscontrol                            
By phone: 888-838-5578 or 703-538-7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

Michelle Butler, FDANEWS, http://www.fdanews.com, +1 (703) 538-7665, [email protected]