Why should you attend:
Since FDA regulations do not allow them to audit your suppliers unless they make finished medical devices, they require that you have sufficient control over them. But from time to time the FDA makes a reinterpretation of what this means. This happened within the last f 5 years, so if you supplier management program is older than that, you need to make major changes in you supplier management program. This is why the Good Manufacturing Practice (aka Quality System Regulations) is called cGMP. The C stands for current, meaning what the FDA considers the current state of the art in the areas they regulate. Also European Notified Bodies also periodically update their expectations, and for suppliers this happened with the publication of a guidance document by the Notified Body Operations Group (NBOG).
This seminar will go into the details of the NBOG supplier guidance document and a GHTF (Global Harmonization Task Force) guidance that describes the current FDA expectation on supplier management.
One of the major things introduced in these guidance document, is the concept of Risk, and the use of identified risks as part of the evaluation and monitoring of suppliers.
This seminar will review requirements and expectation of the FDA and European Notified Bodies for supplier management, and then how to incorporate these into your own supplier management process.
Areas Covered in the Session:
Understand FDA QSR and ISO 13485 requirements for supplier management
Creating a Risk-based Multi-tier supplier classification system
Understand when suppliers have to register and list with the FDA
Defining and using supplier Metrics
Explain the link between design control and purchasing data
Develop an risk-based supplier management process: Incorporating supplier regulatory and safety risk & Incorporating supplier business risk
- Create supplier measurement and monitoring systems
- Understand the how to develop and implement supplier controls
- Create a risk based Value-added system for supplier audits
- How to prepare yourself and your contract manufacturer for unannounced audits from your Notified body
- Creating acceptance criteria and understand how that fits into your supplier control process
Who will benefit:Quality Managers, quality Engineers, Audit Managers, Supplier Engineers, Internal quality auditors, Supplier auditors, Quality associates,Quality Specialists,Regulatory Compliance Managers
Agenda:
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 Corrective Actions
Lecture 8: Evaluating your current program to see how it measures up to regulatory Expectations
Speaker: Betty Lane