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

 
  August 07, 2015  
     
 


Compliance Trainings, Online
2015-08-20


Description :

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.

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 Session:

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

 
 
Organized by: Compliance Trainings
Invited Speakers:

Robert Braido has 40 years of experience in the medical industry. He is president of Visionary Consulting LLC and has been consulting with medical OEM’s and CMOs for over 7 years. Mr. Braido’s has a broad breadth of medical industry experience in prototype/product development, global strategic/tactical planning, technical due-diligence/gap analysis for acquisitions, engineering, operations and business development. He has had great success working at Ethicon Endo-Surgery a J&J Company, Baxter Healthcare, Teleflex Medical, GW Plastics 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 Society of Plastic Engineers Medical Division for over 10 years and elected Chairman of the Medical Division twice.

 
Deadline for Abstracts: 2015-08-19
 
Registration:

For more information about this event please visit

 

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1590

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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