ComplianceOnline

Transferring Medical Device Production to a Contract Manufacturer - Decision Making Process and Procedures

Instructor: Rob Braido
Product ID: 702719
Training Level: Intermediate to Advanced
  • Duration: 90 Min

recorded version

$229.00
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: Oct-2013

Training CD

$299.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This webinar on outsourcing medical device manufacturing will discuss practical decision making steps you can follow to analyze whether to transfer or invest in keeping production in-house. If you decide to transfer production, then this training will detail the options and next steps to transferring it to the right facility or contract manufacturer.

Why Should You Attend:

With the economy, many medical OEMs are deciding whether to invest in upgrading equipment, technology, new personnel, transfer it to a lower cost in-house facility or transfer it to a contract manufacturer. In many cases this could save the OEM from investing in costly bricks and mortar, new technology and higher labor cost. It also frees up floor space for new product initiatives.

This 90-minute webinar will give you the steps to follow in making decisions that could save money, time and people. We will explore the importance of quality, cost and on time delivery/flexibility in making the right decisions. This session will also benefit contract manufacturers, since they have to be ready for a seamless transfer of production by understanding their responsibility and the requirements for a medical device transfer, including the transfer process, validations and the pitfalls that could lead to delays.

Areas Covered in the Seminar:

  • Gap Analysis, Due-diligence and Decision Making.
  • Choosing A Contract Manufacturer.
  • Request for Information (RFI), Request for Proposal (RFP), Request for Quote (RFQ).
  • Supplier Audits.
  • Final Selection & Contract Negotiation.
  • Project Management.
  • Supply Chain.
  • Master Validation Plan.
  • Protocols.
  • Transfer Process.
  • Benefits.
  • Pitfalls.
  • Post Review.
  • Celebrate.

Who will Benefit:

This webinar will provide valuable assistance and give a procedure to the medical device companies that are thinking of transferring production to a contract Manufacturer or transferring it to another facility. The personnel who will benefit include:

At Medical Device OEM's:

  • Decision Makers
  • R&D and Product Development Engineers and Managers
  • Pilot Plant Manager
  • Plant and Production Managers
  • Project and Process Engineers
  • Supply Chain Managers
  • Global Contract Manufacturing Transfer Teams
  • Global Strategic Managers
  • Quality and Validation Teams
  • Quality and Corporate Auditors

At Contract Manufacturers:

  • Decision Makers
  • Contract Manufacturers working in the medical industry
  • Plant and Production Managers
  • Engineering and Contract Manufacturing Transfer Teams
  • Project and Process Engineers
  • Quality and Validation Teams

Instructor Profile:

Mr. Braido, has 40 years of experience in the medical industry. He is the founder and president of Visionary Consulting LLC and has 40 years of medical OEM’s and CMOs to the medical industry. A consulting firm that specializes in gap analysis and due diligence for management evaluation of product transfers, acquisitions and emerging technologies.

Mr. Braido’s has a broad breadth of medical industry experience in, product development, global strategic/tactical planning, technical due-diligence/gap analysis for acquisitions, engineering, operations and strong leadership skills to help develop new product concepts for business and marketing. He has had great success working at Ethicon Endo-Surgery a J&J Company, Baxter Healthcare, GW Plastics, Teleflex Medical and The Tech Group with increasing responsibilities to the level of VP of Advanced Technologies. He was a member of the Board of Directors for the SPE (Society of Plastic Engineers) Medical Division for over 10 years and elected Chairman of the Medical Division twice.

Mr. Braido was selected as a member of a Johnson & Johnson Integration Team that took a small fledgling company with totally new products, technologies and structure from $75 million to $850 million in 5 years. His career is built on the ability to motivate, lead and coach people in different disciplines throughout the medical industry. The key factor has been driving innovation.

While working for J&J he was elected, as the Consortium Chairman for the Government Reinvestment Program with MIT, the National Science Foundation and seven leading Fortune 200 companies to commercialize 3D Printing and emerging technologies in metal and plastics. He has also been an independent reviewer for the National Science Foundation, J&J, MIT, EdgeOne Medical, Beeken Medical and others.

He has published numerous technical and leadership articles and white papers. In the past he has shared his extensive experiences at seminars, workshops, technical conferences, symposiums and webinars on subjects relating to the medical industry on due-diligence/gap analysis, product development, product and equipment transfers, leadership and developing an innovation culture for product concept.

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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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