How to Decommission a Medical OEM Molding Operation and Transfer it to a “World Class” Medical Contract Manufacturer

This webinar will provide processes and procedures to all medical device companies that are thinking of transferring equipment, molds, dies, systems and processes to contract manufacturers. It will follow a recent successful case study in the medical industry.

Why Should You Attend:

The medical industry is in transition. OEM's are in the process of transferring more product and operations to contract manufacturers. Some OEM's and contract manufacturers are struggling with how to deal with these transfers and validation standards.

This medical device webinar will provide valuable assistance and give a process and procedures to all regulated companies that are thinking of transferring equipment, molds, dies, systems and processes to contract manufacturers. It will guide you on how to choose the right world class contract manufacturer. It will also cover how important a master validation plan is to meet today’s standards for the FDA and CE Mark.

Areas Covered in the Seminar:

• Should a medical company decommission and/or transfer an operation to a world class contract manufacturer.
• Gap analysis.
• Choose a world class manufacturer.
• Cost of validation.
• Risk plan.
• Contract negotiation.
• Master validation plan.
• Mold and component transfer.

Who will Benefit:

This webinar will provide valuable assistance and give a process and procedure to regulated companies to either keep operations inside or transfer equipment, molds, dies, systems and processes to a contract manufacturer.

• Plant managers and operation personnel in the medical industry (OEM's and suppliers)
• Project management teams
• Strategic supply chain teams
• Manufacturing engineers
• R&D, product development engineers and managers associated with validations
• QA, Regulatory Affairs and team members
• Validation specialists