ComplianceOnline

Qualification of Contract Manufacturer Organizations Based on Practical Experience

Instructor: Edwin Waldbusser
Product ID: 705384
  • 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: Sep-2017

Training CD / USB Drive

$349.00
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

This webinar will cover in detail the steps to plan and conduct a program to qualify contract manufacturer organizations (CMOs). It will teach best practices to meet regulatory requirements and satisfy practical needs to obtain the best CMO.

Complimentary Hand-outs:

For easy implementation, attendees will receive:

  • 6 page CMO pre-audit quality survey form
  • 25 page CMO audit survey form

Why Should You Attend:

Regulatory agencies require that companies carefully select suppliers and contract manufacturers. The responsibility for product quality and safety remains with the company. It cannot be delegated to the Contract Manufacturing Organization (CMO). CMO’s must be selected following a rigorous formalized procedure.

This webinar will describe a compliant program based on regulatory requirements and the author’s personal experience in qualifying over 40 CMO’s in the medical device industry.

Areas Covered in the Webinar:

  • CMO management principles
  • Supplier quality categories
  • Approved Vendor List (AVL)
  • Phases of CMO selection from initial telephone inquiry to quality survey to qualification audit
  • Planning a qualification audit-establishing evaluation team
  • Conducting a qualification audit-key points to evaluate
  • Decision factors for selecting a CMO-key practical points
    • Distinctive technical competence
    • Optimum CMO size
    • Risk of educating future competitor
  • Key points for the contract
  • Change approval by both CMO and company
  • Quality Agreement
  • Dealing with uncooperative suppliers

Who Will Benefit:

  • Engineering personnel
  • QA personnel
  • Software developers
  • Project managers
  • Regulatory affairs professionals
  • Global contract manufacturing transfer teams
Instructor Profile:
Edwin Waldbusser

Edwin Waldbusser
Regulatory Consultant, Med Device Advisors

Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the areas of design control, risk analysis and software validation for the past 8 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.

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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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