ComplianceOnline

Integrating Risk Management with Supplier Management

Instructor: William G Mclain
Product ID: 700384
Training Level: Intermediate
  • Duration: 60 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: May-2007

Training CD / USB Drive

$500.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

In this Medical device training we will discuss methods for documenting and demonstrating control over your suppliers. Emphasis is placed on identifying and implementing these controls, not just auditing to establish compliance.

Description

Medical device manufacturers increasingly rely on outsourcing significant portions of their operations. It is now quite common for much of a quality management system to be outsourced to suppliers.

Worldwide regulatory agencies expect the modern medical device manufacturer to demonstrate control over these suppliers. This level of control will vary given the risk of the service provided. In this session we will discuss methods for documenting and demonstrating control over your suppliers. Emphasis is placed on identifying and implementing these controls, not just auditing to establish compliance.

Areas Covered in the seminar:

  • Scope and scale of supplier management
  • Current regulatory expectations of supplier management
  • The use of a Supplier management Plan
  • Methods to minimize the need for supplier audits

Who Will Benefit:

  • RA/QA Managernt
  • Procurement engineers
  • Purchasing
  • Quality engineering
  • Product Development engineering
  • Anyone who outsources components, products or services in the medical device industry

Instructor Profile:

William G. Mclain, RAC, B.S.E. is the President and Principal Consultant for Keystone Regulatory Services, LLC. He has over 15 years experience in product development, domestic and international regulatory affairs and risk management, and quality management system design in the medical device industry. He has contributed to the timely development and market introduction of cardiovascular, anesthesiology, gastroenteral, diagnostic and general surgical devices by providing regulatory, quality system and risk management strategy, oversight, and support. An active member of RAPS and ASQ Biomedical Division, Mr. McLain is RAC Certified and holds a BS in Mechanical Engineering from Grove City College.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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