This is a 4-day training see recurring event

Who Should Attend: This course is recommended for anyone involved in designing, implementing, maintaining and improving a quality management system and/or performing internal audits of a quality management system, such as quality officers, managers and auditors. No prior knowledge of auditing, quality management systems or ISO 9001:2008 is required prior to attending this course.

Course Highlights / Topics Covered:

• The process approach, performance indicators and risk
• The "Plan-Do-Check-Act” principle
• The key elements of a quality management system, management of documents/records, deviations, corrective and preventive actions
• Management responsibility, management representative and management review
• Measurement, analysis and continuous improvement on customer satisfaction, quality management effectiveness through internal audits, process performance and conformity to product requirements
• What are internal audits
• Why are internal audits conducted
• What preparatory work should be carried out before an audit
• What to pay attention to during the audit
• What is a good audit report
• What aspects are important in monitoring audit results, corrective and preventive actions

Students will benefit by:

• Learning how to plan, conduct, and report quality audit results
• Enhancing your understanding of the components of an internal quality audit program
• Gaining an in-depth understanding of ISO 9001 requirements
• Getting answers to your toughest audit questions

Capturing a working knowledge of the practices, roles and responsibilities of an auditor

GROW AND PROTECT YOUR BUSINESS’ MEDICAL DEVICE SALES THROUGH MEDACCRED AND MEDMMAP: Webinar 3 of 4 with Edwards LifeSciences & Kimball Electronics

Are you targeting the medical device market as part of your business’ growth plans?

Possibly searching for ways to diversify your sales?

Or maybe your company is heavily invested in the medical device market and needs to protect its revenue base and maintain competitiveness?

The MedAccred certification and the supporting MedMMAP program -Medical Manufacturers MedAccred¨ Accreditation Pathway (MedMMAP)–may help accelerate your business plans in the medical device sector while improving your critical processes.OEMs, who started the program in 2012to reduce product recalls, are increasingly requiring the MedAccred certification from their supply chains to maximize patient safety and improve quality. Suppliers who have earned the certification note their sales growth, reduced costs related to scrap and rework, and increased prospects across the medical device sector.The national network of Manufacturing Extension Partnerships –MEP Centers –is managing the government-fundedMedMMAP program to help manufacturers, who are strategically growing in the medical device sector, to get started with their MedAccred certification. Selected businesses will become part of the MedMMAP program and work with MEP subject matter experts on evaluating their critical processes and help them prepare for certification by the Performance Review Institute (PRI) for MedAccred. PRI is the exclusive non-profit accreditor for NADCAP –commonly used in the aerospace and defense industry since the 1990s –and MedAccred.Don’t take our word for it. Please register for one of our free webinar events to learn more about MedAccred and MedMMAP from OEMs driving the certification, suppliers who earned the accreditation, and MEP Centers (Manufacturing Extension Partnerships) supporting manufacturers throughout the country.Hear directly from executives why OEMs view this accreditation as critical to the future of their supply chains and how MedMMAP and MedAccred have transformed how they do business in the medical device industry.

Click on this Link to register!