About Supplier Management for Medical Device Manufacturers 2018
Supplier Management for Medical Device Manufacturers Seminar is going to start on 12 Mar and finish on 13 Mar 2018.
The calls you to Zurich, for Supplier Management for Medical Device Manufacturers Seminar. The Course, takes place at Hilton Zurich Airport.
Supplier Management for Medical Device Manufacturers 2018 is likely to be a platform where lots of significant products will probably be showcased. Many of these are about Medical Devices, Medical Device Manufacturers and Supplier Management.
Supplier Management for Medical Device Manufacturers Seminar is three times a year Course.
Global Compliance Panel is the PCO of Supplier Management for Medical Device Manufacturers 2018, Supplier Management for Medical Device Manufacturers Seminar.
Let Zurich must do visitor attractions make you adore this city when you are there for Supplier Management for Medical Device Manufacturers 2018. Here are the great things you can do in Zurich!
Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the device manufacturer, which means that they can be critical to performance and delivery of your device. Neither the FDA nor your notified body regulates your suppliers (with a few exceptions). They expect you to have an effective process to ensure your suppliers perform in the regulatory environment. How well do you understand the requirements for supplier management? Could you pass a regulatory audit or inspection without any issues? This course delivers the tools, templates, and methods to help participants implement an effective and efficient supplier management program. This two-day hands-on course provides a clear understanding of the underlying principles of supplier management. The course uses exercises to solidify understanding. In addition, the course uses FDA Warning Letters to illustrate the points and help you learn from others
Important Dates
Day 1 Schedule
Lecture 1: Introductions
Lecture 2: Fundamentals Regulatory Requirements FDA Requirements ISO 13485 requirements Understanding the role of the Global Harmonization Task Force Guideline Understanding NBOC Guideline and why it should be used
Lecture 3: Planning the Supplier Management Program Supplier Classification Supplier QA agreements what are they and why are then
Day 2 Schedule
Lecture 1: Planning Supplier Selection
Lecture 2: Potential Suppliers
Lecture 3: Supplier Selection
Lecture 4: Implementing Supplier Controls
Lecture 5: Monitoring, Measuring, and Evaluation Periodic Monitoring Re-evaluations
Lecture 6: Supplier Audits - where do they add value Planning your supplier audit schedule How Notified Body unannounced audits affect your contract manufacturer What you should do to prepare yourself and your contract manufacturer for unannounced Notified body audits
Lecture 7: Feedback and Communication Supplier meetings: Partnering with Key suppliers Supplier
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