GROW AND PROTECT YOUR BUSINESS’ MEDICAL DEVICE SALES THROUGH MEDACCRED AND MEDMMAP

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 2012 to 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-funded MedMMAP 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.

Session 1 – March 23, 2-3pm CST

• Dannette Crooms, Sr. Director of Global Supplier Quality, Edwards Lifesciences
• Jim Rigney, Director of Quality, TG3 Electronics

Session 2 – March 26, 2-3 CST

• Scott Goolsbey, Supplier Controls Manager, Stryker
• Bryan Barrera, Chief Operating Officer, Trademark Plastics

Session 3 – March 30, 2-3pm CST

• Dannette Crooms, Sr. Director of Global Supplier Quality, Edwards Lifesciences
• Jay Matthews, Quality Manager, Kimball Electronics

Session 4 – April 1, 2-3pm CST

• Scott Goolsbey, Supplier Controls Manager, Stryker
• Alex Hoffer, Chief Revenue Officer, Hoffer Plastics