Techniques for Medical Device Packaging 2017



Accelerated aging (AA) is testing that uses aggravated conditions of heat, oxygen, sunlight, vibration, chemicals, etc. to speed up the normal aging processes of items. It is used to help determine the long-term effects of expected levels of stress within a shorter time, usually in a laboratory by controlled standard test methods.

Why should you Attend:

Accurate prediction of product shelf-life performance is critical to your success. "Do it right the first time", choose the most functional and resistant materials for your product instead of going through the post launch cycle of panic driven product revisions. Also learn the basis for choosing the optimum accelerated test design based on materials, product design, processing, and functional product requirements. Learn how to "think like a molecule" and plan and design around "aging" induced changes in materials qualities (brittleness, color, and odor) that cut short your product's long term functionality. The understanding of a product's long term safety and efficacy is a must in today's litigious world.

Areas Covered in the Session:

  • Shelf Life Test Methods - Accelerated Aging Test Design - Modeling
  • General Aging Theory - Simplified Protocol
  • Accelerated Aging Test Designs
  • Polymers Chemistry - choosing the best polymer candidate
  • Product Validation and Verification (ISO9001)
  • Regulatory (i.e. FDA) Acceptance and Legal Considerations

Who Will Benefit:

  • Product Design Engineers
  • Quality Management and Engineers
  • Regulatory Affairs
  • Project Managers
  • Staff evaluating risk, safety, and effectiveness
  • R&D Staff - engineering and lab personnel
  • Process Engineers
  • Packaging Engineers
  • Materials Engineers
  • Manufacturing Engineers
  • Liability - Lawyers, Paralegals

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]

Speaker and Presenter Information

Karl Hemmerich
President at Ageless Processing Technologies
Karl J Hemmerich has over 35 years of experience in medical device product design, development, manufacturing, and sterilization. He specializes in sterilization method selection and program development with emphasis on component material selection, process development and sterilization process validation.

Relevant Government Agencies

Medical Device Packaging


Event Type
Webcast


This event has no exhibitor/sponsor opportunities


When
Thu, Feb 2, 2017, 10:00am - 11:00am PT


Cost

General admission:  $150.00


Website
Click here to visit event website


Organizer
NetZealous - Compliance4All


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