Radiation Sterilization of Medical Devices

Radiation Sterilization of Medical Devices

Online event
Tuesday, Aug 25 at 9 am to Wednesday, Aug 26 at 1 pm EDT
Overview

Radiation Sterilization of Medical Devices; 1.5 Training Session, Virtual Training; August 25-26, 2026

Schedule (all times EST)

  • Day 1: 9:00am - 5:00pm
  • Day 2: 9:00am - 1:00pm

About the training

Cleaning is often a critical step in the manufacturing process of single-use medical devices as contaminants could cause serious safety problems as well as impact device biocompatibility and sterilization effectiveness. It is the responsibility of the medical device manufacturer to ensure physical, chemical and microbiological contaminants (as applicable) are reduced to a safe level and to provide objective evidence of the verification of the cleaning process effectiveness.

Implementing an effective cleaning process on medical devices requires knowledge on the cleaning technologies available, process design, risk management, test methods, cleanliness requirements, process validation, and process verification. These topics will be covered in this comprehensive course with a focus on NF ISO 19227:2018.


REQUIRED LEVEL

Some familiarity with process validation (such as OQ/PQs) and general knowledge of medical devices manufacturing.


To learn more about the program, click here.

Radiation Sterilization of Medical Devices; 1.5 Training Session, Virtual Training; August 25-26, 2026

Schedule (all times EST)

  • Day 1: 9:00am - 5:00pm
  • Day 2: 9:00am - 1:00pm

About the training

Cleaning is often a critical step in the manufacturing process of single-use medical devices as contaminants could cause serious safety problems as well as impact device biocompatibility and sterilization effectiveness. It is the responsibility of the medical device manufacturer to ensure physical, chemical and microbiological contaminants (as applicable) are reduced to a safe level and to provide objective evidence of the verification of the cleaning process effectiveness.

Implementing an effective cleaning process on medical devices requires knowledge on the cleaning technologies available, process design, risk management, test methods, cleanliness requirements, process validation, and process verification. These topics will be covered in this comprehensive course with a focus on NF ISO 19227:2018.


REQUIRED LEVEL

Some familiarity with process validation (such as OQ/PQs) and general knowledge of medical devices manufacturing.


To learn more about the program, click here.

Good to know

Highlights

  • 1 day 4 hours
  • Online

Refund Policy

Refunds up to 14 days before event

Location

Online event

Organized by
GMED North America, Inc.
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