Handling, Storage, Distribution, and Installation of Medical Devices 2016

Topics

• Preventing Mix-ups, damage, deterioration, contamination
• Handling processes
• Environmental controls
• Storage requirements including stock rotation
• When a product`s fitness for use / quality deteriorate over time
• Authorizing receipt and dispatch from storage areas
• Installation procedures including inspection and testing
• Identification of products
• Important linkages to other QMS requirements

Who should Attend

Attendees from:

• Document Control Specialists
• Quality Systems Specialists
• Internal Auditors and Managers
• Quality and Compliance Specialists
• Quality/Compliance managers or directors for Medical Device companies
• CAPA Specialists
• Operations, Distributions personnel wanting to learn how to understand Quality System requirements