New York Professional Events List


Supplier Management in FDA- and ISO-regulated Industry


Date
Sep 14, 2017 - 09:00 AM - Sep 15, 04:00 PM
Organizer
Global Compliance Panel
Location
DoubleTree by Hilton Hotel San Diego Downtown 1646 Front St, San Diego, CA 92101, USA,

San Diego,
CA,
US,
ZIP: 92101
Phone: 1 929 900 1853

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
    • Review of FDA requirements
    • Review of ISO requirements
    • Types of suppliers that must be qualified
    • Defining critical suppliers
    • Outsourced processes
    • Recommended Practices
    • Documentation requirements
    • Use of Risk Assessment
    • The Quality Agreement
    • Common Pitfalls
  • Supplier Assessment
    • Review of FDA requirements
    • Review of ISO requirements
    • Case Study: A Hypothetical Supplier Assessment
    • Recommended Practices
    • Documentation requirements
    • Use of Risk Assessment
    • Common Pitfalls
  • Supplier Nonconformance
    • Types of supplier nonconformances
      • Best Practices for Notification
      • Best Practices for Handling
      • Trending
      • Evaluation of Supplier Response
      • Tracking effectiveness
    • 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
---------------------------------------------------------------------
Please contact the event manager Marilyn below for the following:
- For Registrations Please call +1 929.900.1853
- Discounts for registering 5 or more participants.
- If you company requires a price quotation.
Event Manager Contact: marilyn.b.turner(at)nyeventslist.com
You can also contact us if you require a visa invitation letter, after ticket purchase.
We can also provide a certificate of completion for this event if required.
 
NO REFUNDS OR TRANSFER ALLOWED ON REGISTRATIONS
-----------------------------------------------------------------
This Event Listing is Promoted by
New York Media Technologies LLC in association
with NetZealous LLC.

http://www.NyEventsList.com
http://www.BostonEventsList.com
http://www.SFBayEventsList.com
-----------------------------------------------------------------
JAI170516EVZTODAY

 


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
Best Practices for Handling
Best Practices for Notification
Trending
Evaluation of Supplier Response
Tracking effectiveness

Lecture 2: 
Supplier Nonconformance (cont)
Supplier Corrective Action Requests
Pre-notification?
Best Practices for Issuance
Followup
Evaluation/Acceptance of Supplier Response
Tracking effectiveness

Lecture 3: 
Workshop
Acceptability of Supplier Responses

Lecture 4: 
Q&A - Conclusion
 

 


Speaker Details


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.


Event Categories
BUSINESS & MANAGEMENT CONFERENCES
,
Technology
Keywords: fun, assessment , class , Fun , implement, industry , Management , program , purchase, sin




Comments








Events Calendar

SunMonTueWedThuFriSat
27 28 29 30 31 1 2
3 4 5 6 7 8 9
10 11 12 13 14 15 16
17 18 19 20 21 22 23
24 25 26 27 28 29 30

Event Location

Newsletters

Subscribe
VIP Life Time Subscription to our Newsletters!
$399.99
$299.99