Polymer Materials Selection for Radiation-Sterilized Products



Overview:

Review of basic polymer chemistry and changes in polymer characteristics can be anticipated and designed for. Learn how to plan for post radiation resistance and lifetime functionality. All radiation modalities (gamma, e-beam, x-ray) will be reviewed for a basic understanding of the sterilization process and the influences that product design and assembly can have on success.

 

The following subjects will be covered in detail:

  • Materials Guidance's - AAMI TIR # 17, ASTM
  • Sterilization validation and Bioburden
  • Shelf Life Test Methods - Accelerated Aging design
  • Product design
  • The influences of product assembly (molding, automation, etc.)'
  • Material selection and post irradiation degradation
  • Regulatory Guidance's - AAMI/ISO 11137, TIR #17
  • Packaging Design and Materials

Why should you Attend:

"Do it right the first time", choose the most functional and radiation resistant materials for your medical device instead of going through the post launch cycle of product revisions. Also learn the basis for choosing the optimum sterilization modality based on materials, product design, bioburden, and logistics. Learn how to "think like a molecule" and plan and design around radiation induced changes in materials qualities (color, odor, brittleness). How to avoid the materials that are "APT" to fail.


Learn how to:

  • Identify the materials that perform best upon radiation
  • Keep color and odor out of your irradiated products
  • Enhance product and packaging designs to take advantage of radiation
  • Which modality (Gamma, E-beam, X-ray) will perform best for my product

Areas Covered in the Session:

  • Polymers Chemistry - choosing the best polymer candidate
  • Gamma, E-beam, X-ray sterilization
  • Accelerated Aging
  • Product Validation
  • Sterilization Validation - Establishing the baseline dose (VDmax)

Who Will Benefit:

  • Medical product design Management and Engineers
  • Sterilization Experts
  • Quality Management and Engineers
  • Regulatory Affairs
  • Project Managers
  • Purchasing and Supply Chain Managers
  • Staff evaluating risk, safety, and effectiveness
  • R&D Staff - engineering and lab personnel
  • Process Engineers
  • Packaging Engineers
  • Materials Engineers
  • Manufacturing Engineers

Contact Details:

Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: [email protected]
http://www.compliance4all.com/
Event Link : http://bit.ly/29nErWP
LinkedIn Like us – https://www.linkedin.com/company/compliance4all-trainings
Twitter Follow us – https://twitter.com/compliance4all
Facebook Like us – https://www.facebook.com/Compliance4all
Pinterest - https://in.pinterest.com/compliance4all/

Speaker and Presenter Information

Karl LeinsingKarl Leinsing has experience with design and project management since 1988 and has been in the Medical Product Device Design and Development industry since 1992. His areas of expertise include full life cycle product development, product conception, polymer selection, thorough computer-aided product design, dynamic mechanical analysis and root cause analysis, molding and manufacturing, project organization, technical presentations and leadership, and cross-functional teamwork. Karl currently holds 19 patents (several patents pending), 5 design awards, was listed as one of "100 notable people in the Medical Device Industry" by Medical Device and Diagnostic Industry (MDDI), and was inducted into the Product Design & Development Engineer Hall of Fame.

Relevant Government Agencies

Radiation-Sterilized


Event Type
Webcast


This event has no exhibitor/sponsor opportunities


When
Wed, Aug 10, 2016, 10:00am - 11:00am PT


Cost

Individual:  $150.00
Recording only:  $190.00
Corporate:  $290.00
Corporate recording only:  $390.00


Website
Click here to visit event website


Organizer
NetZealous - Compliance4All


Contact Event Organizer


Join the event conversation:
@Compliance4all
#Compliance4all


Return to search results