Supplier Management in FDA 2017 - Supplier Management in FDA- and ISO-regulated Industry 2017

Course "Supplier Management in FDA- and ISO-regulated Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Overview:
Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance. Many companies can spend significantly less time and money, and still be in control of their suppliers and in compliance with the regulations. This class will review the QSR and ISO requirements for supplier evaluation, including defining the types of suppliers that require evaluation. The QSR/ISO requirements for supplier assessment will be defined as well. Attention will be paid to inclusion of risk management in across both supplier qualification and assessment, implementation of which will allow your company to devote value-added resources to these efforts. Significant time will be spent on discussion of the topic of supplier nonconformance, including how and when to issue the dreaded Supplier Corrective Action Request. Your supplier nonconformance handling process must be nonconfrontational, or even better, collaborative. If your company is too demanding of your suppliers, you risk alienating them or even worse losing them - try explaining that to your supply chain folks.
Why should you attend
Notified bodies and the FDA cannot require your suppliers to meet the quality system regulations, so they must make sure you are exercising sufficient control over those suppliers. You must make sure your supplier management and system meets all required regulations and guidance documents, especially for outsourced processes such as contract manufacturing, sterilization and testing, and also for critical suppliers. Sure, you depend on your suppliers to provide you with goods and services, but can your system prove that you have sufficient control over your suppliers to assure auditors and regulatory agencies that your product is safe and meets all your requirements? Your supplier management program can be in compliance, but is it cost effective? If not, your unquantifiable overhead costs may be out of control. Is your supplier management program collaborative with your suppliers? If your company is too demanding of your suppliers, you risk alienating them or even worse losing them - try explaining that to your supply chain folks!
Areas Covered in the Session:
• Supplier Selection
o Review of FDA requirements
o Review of ISO requirements
o Types of suppliers that must be qualified
o Defining critical suppliers
o Outsourced processes
o Recommended Practices
o Documentation requirements
o Use of Risk Assessment
o The Quality Agreement
o Common Pitfalls
• Supplier Assessment
o Review of FDA requirements
o Review of ISO requirements
o Case Study: A Hypothetical Supplier Assessment
o Recommended Practices
o Documentation requirements
o Use of Risk Assessment
o Common Pitfalls
• Supplier Nonconformance
o Types of supplier nonconformances
 Best Practices for Notification
 Best Practices for Handling
 Trending
 Evaluation of Supplier Response
 Tracking effectiveness
o Supplier Corrective Action Requests
 Pre-notification?
 Best Practices for Issuance
 Followup
 Evaluation/Acceptance of Supplier Response
 Tracking effectiveness
• Workshop: Review of Supplier Responses: Acceptable or UNacceptable?
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that are interested in implementing and maintaining a supplier management program that is both compliant and cost-efficient. The employees who will benefit include:
• Supply chain management
• Buyers
• Purchasing management
• CAPA Coordinators
• Regulatory management
• QA management
• Executive management
• Internal auditors
Agenda:
Day 1 Schedule
Lecture 1: Introduction
Supplier Selection
• Review of FDA requirements
• Review of ISO requirements
• Types of suppliers that must be qualified
• Defining critical suppliers
• Outsourced processes
Lecture 2:
Supplier Selection (cont)
• Recommended Practices
• Documentation requirements
• Use of Risk Assessment
• The Quality Agreement
• Common Pitfalls
Lecture 3:
Supplier Assessment
• Review of FDA requirements
• Review of ISO requirements
• Case Study: A Hypothetical Supplier Assessment
• Recommended Practices
Lecture 4:
Supplier Assessment (cont)
• Documentation requirements
• Use of Risk Assessment
• Common Pitfalls
Day 2 Schedule
Lecture 1:
Supplier Nonconformance
• Types of supplier nonconformances
o Best Practices for Handling
o Best Practices for Notification
o Trending
o Evaluation of Supplier Response
o Tracking effectiveness
Lecture 2:
Supplier Nonconformance (cont)
• Supplier Corrective Action Requests
o Pre-notification?
o Best Practices for Issuance
o Followup
o Evaluation/Acceptance of Supplier Response
o Tracking effectiveness
Lecture 3:
Workshop
• Acceptability of Supplier Responses
Lecture 4:
Q&A - Conclusion
Speaker
Jeff Kasoff
Director of Regulatory Affairs, Life-Tech, Inc
Jeff Kasoff, RAC, CMQ/OE has more than 30 years in Quality and Regulatory management. Over that time, Jeff has implemented and overseen quality system operations and assured compliance, at all sizes of company, from startup to more than $100 million in revenue. This multi-faceted experience makes Jeff uniquely qualified to address compliance issues across the entire range of company sizes. Jeff has also been primary liaison with FDA inspectors and notified body auditors, giving him first-hand experience with the most common issues surfaced by regulatory agencies. Jeff received his Regulatory Affairs Certification from RAPS , his Manager of Quality and Organizational Excellence certification from ASQ, and his Lean Black Belt from IIE.
Location: San Diego, CA Date: September 14th & 15th, 2017 and Time: 9:00 AM to 4:00 PM
Venue: DoubleTree by Hilton San Diego Downtown 1646 Front St, San Diego, CA 92101, USA
Price:
Register now and save $200. (Early Bird)
Price: $1,295.00 (Seminar Fee for One Delegate)
Until August 10, Early Bird Price: $1,295.00 From August 11 to September 12, Regular Price: $1,495.00
Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar
At this seminar, world-renowned FDA Regulated Industry subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about FDA Regulated Industry and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to FDA Regulated Industry.
As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in FDA Regulatory -related industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.
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