Designing a Supplier Qualification Program: One and a Half-day In-Person Seminar

Expired
Dates : 19 July 2016 » 20 July 2016

Place : San Francisco
United States

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Organizer :

Engineering and Technology;
Keywords: Design, Manufacturing
Description :

 

Course Description:

Manufacturers bear the responsibility for every step in their supply chain to ensure they provide quality finished medical devices beyond what can be achieved through testing and inspection, meaning overall quality depends on quality of raw materials, components and services. In addition, manufacturers must make sure that all aspects of the supply chain are compliant with regulatory and quality system requirements. To do this, it is critical that manufacturers evaluate and approve product and service suppliers prior to issuing a Purchase Order, but what is a supplier qualification program?

This 1.5-day seminar outlines the supplier qualification process and requirements and provides how-to information for designing (or redesigning) a sustainable and regulatory compliant supplier qualification program.

 

 

 

Learning Objectives:

Upon completing this course, participants should be able to:

  • Define the requirements for a sustainable and regulatory compliant supplier program
  • Explain how change controls, quality plans and other quality programs feed into the supplier qualification program
  • Apply risk-based approaches to the supplier selection process and incorporate into a quality management system
  • Create audit checklists, supplier assessments, scorecards and other qualification tools to use in the pre-selection, selection and assessment process
  • Document approve supplier lists, supplier agreements, quality agreements and other supplier documentation
  • Classify, rank, monitor, re-qualify, and disqualify suppliers through performance measurements
  • Conduct on-site and off-site verifications

 

Who will Benefit:

This course is designed for people responsible for following purchasing procedures, those tasked with developing and improving purchasing and supplier controls including approval of suppliers, components, raw materials and services, and individuals responsible for quality management system improvements and compliance.

Following personnel will benefit from the course:

  • Quality professionals
  • Regulatory professionals
  • Compliance professionals
  • Purchasing supervisors
  • Manufacturing engineers
  • Design engineers
  • Quality engineers
  • Document control specialists

 

 

Note:

Use coupon code NB5SQH8N and get 10% off on registration.

 

For Registration:

http://www.complianceonline.com/supplier-qualification-program-fda-qsr-qms-iso-13485-seminar-training-80392SEM-prdsm?channel=sciencedz  

 

 

 


Designing a Supplier Qualification Program: One and a Half-day In-Person Seminar to be held in San Francisco, United States between 19 July 2016 and 20 July 2016. It covers specific areas of Biology and life sciences such as . Visit the website of the conference for more detailed information or contact the organizer for specific questions.
Add to calendar 2016-07-19 2016-07-20 Europe/London Designing a Supplier Qualification Program: One and a Half-day In-Person Seminar https://www.sciencedz.net/en/conference/21061-designing-a-supplier-qualification-program-one-and-a-half-day-in-person-seminar San Francisco - United States

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