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Webinar On Due-diligence and Gap Analysis in Decision Making Process for Medical Companies

 
  February 27, 2015  
     
 


Compliance Trainings, Canada
2015-03-17


Description :

In this seminar, we will discuss practical decision making steps you can follow to analyze whether to transfer or invest in keeping production in-house from a successful case study.  If it is decided to transfer production what are the options and next steps to transferring it to the right facility or contract manufacturer (CMO).

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/Inventory

Master Validation Plan

Protocols/Validations

Transfer Process to an in-house facility or Contract Manufacturer

Benefits

Pitfalls

Post Review/Lessons Learned

Who Will Benefit:

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

Medical Device OEM’s

OEM and Contract Manufacturing (CMO) Senior Management

Decision Makers in regulated industries

R&D and Product Development Engineers and Managers

Business Development

Pilot Plant Manager

Operations Managers

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

Contract Manufacturers

Decision Makers in regulated industries

Business Development

Contract Manufacturers

Plant and Production Managers

Operation Managers

Engineering and Contract Manufacturing Transfer Teams

Project Management Teams

Project and Process Engineers

Quality and Validation Teams

Price tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

Like Us On Facebook:

https://www.facebook.com/events/799538343447374/?source=1&sid_create=2522263151 

 
 
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: 2015-03-17
 
Registration:

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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