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

  February 08, 2013  
ComplianceOnline, Online Event

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.
Organized by: Complianceonline
Invited Speakers: Rob Braido, is the founder and principle of Visionary Consulting LLC, a consulting firm that specializes in gap analysis and due diligence for management evaluation of product transfers, acquisitions and emerging technology. Visionary Consulting also specializes in the project management of validated processes and equipment for product transfers in the medical device and surgical instrument market.

Mr. Robert Braido has 40 years of experience in the medical industry. He has been consulting and training medical OEM’s and suppliers to the medical industry for the last seven years.

Mr. Braido’s has a broad breadth of industry experience in prototype/product development, global strategic/tactical planning, technical due diligence/gap analysis, engineering and strong leadership skills to help develop new products and businesses. He has had great success working at Ethicon Endo-Surgery a J&J Company, Teleflex Medical, The Tech Group and Baxter Healthcare with increasing responsibilities to the level of VP of Advanced Technologies. He was a member of the Board of Directors for the SPE Medical Division for over 10 years and elected Chairman of the Medical Division twice.
Deadline for Abstracts: 2013-03-13
Registration: For Reg: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702719?channel=Hummolgen
E-mail: referral@complianceonline.com
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