Thanks! You've successfully subscribed to the BONEZONE®/OMTEC® Monthly eNewsletter!

Please take a moment to tell us more about yourself and help us keep unwanted emails out of your inbox.

Choose one or more mailing lists:
BONEZONE/OMTEC Monthly eNewsletter
OMTEC Conference Updates
Advertising/Sponsorship Opportunities
Exhibiting Opportunities
* Indicates a required field.

How to Improve Supplier Scorecards

 Buyer/Planner    Materials/Commodity Manager   ● Purchasing
● 
Quality Control    Supply Chain Management  


                                                                                           Mr. Packard will also present on Design Planning.

This presentation educates OEMs and suppliers alike. OEMs will learn how to collect data to create a more useful supplier scorecard without wasting precious human resources, and suppliers will learn how to interpret scorecards so that they understand where they need to improve. You will learn about common mistakes that frequently result in discrepancies between perceived excellence and a poor supplier score. You will also learn how scorecards can be ignored and even become a compliance liability.

Session Takeaways:

• What should be measured?
• How often should scorecards be issued?
• What’s an acceptable score?
• What should you do if you disagree with a score?
• What should you do if your supplier ignores a poor score?

Rob-Packard WEBRobert Packard
Founder
Medical Device Academy

Robert Packard is a regulatory consultant with 20 years of experience in the medical device, pharmaceutical and biotechnology industries. He is a graduate of UConn in Chemical Engineering. Mr. Packard served in senior management at several medical device companies, including President/CEO of a laparoscopic imaging company. His Quality Management System expertise covers all aspects of developing, training, implementing and maintaining ISO 13485 and ISO 14971 certification. From 2009 to 2012, he was a lead auditor and instructor for one of the largest Notified Bodies. Mr. Packard's specialty is regulatory submissions for high-risk medical devices, such as implants and drug/device combination products for CE marking applications, Canadian medical device applications and 510(k) submissions. The most favorite part of his job is training others.