Medical Devices 2011 - Sterilization Options for Challenging Products
Date2011-05-26
Deadline2011-05-26
VenuePalo Alto, USA - United States
KeywordsMedical Devices,conference,event,Webinar
Topics/Call fo Papers
Why Should You Attend:
Medical products are more complicated and have greater challenges for sterilization process than ever before. These products might include tissue-based products, combination products, devices with drug coatings, devices with batteries or equipped with integrated software, circuits or computer chips.
Each of these present their own challenges for sterilization starting with selecting a compatible process to developing the validation strategy and meeting the regulatory requirements for ensuring that the sterilization process is adequate for the medical product. Making a mistake can be costly not only in immediate costs but also in project delays and potentially in regulatory approval.
This presentation will review various sterilization processes and their general compatibility to various types of challenging medical products as well as some of the challenges that each of the various sterilization processes might present. In addition the methods that are available for validation will be addressed demonstrating how they may be applied to reduce the effects of the sterilization process.
NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Medical products are more complicated and have greater challenges for sterilization process than ever before. These products might include tissue-based products, combination products, devices with drug coatings, devices with batteries or equipped with integrated software, circuits or computer chips.
Each of these present their own challenges for sterilization starting with selecting a compatible process to developing the validation strategy and meeting the regulatory requirements for ensuring that the sterilization process is adequate for the medical product. Making a mistake can be costly not only in immediate costs but also in project delays and potentially in regulatory approval.
This presentation will review various sterilization processes and their general compatibility to various types of challenging medical products as well as some of the challenges that each of the various sterilization processes might present. In addition the methods that are available for validation will be addressed demonstrating how they may be applied to reduce the effects of the sterilization process.
NOTE: Use This Promocode ( 117660 ) To Get 10% Discount.
Other CFPs
- The Use and Mis-use of FMEA in Medical Device Risk Management
- The FDA’s (MDDS)final rule and its implications for currently regulated and unregulated vendors and providers
- You have a sterility or Bioburden test failure
- Process Validation for Medical Device Manufacturers
- The 510(k) Process and Risk Management
Last modified: 2011-03-11 19:23:10