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ISO 17665:2006 Training

Our training program emphasizes ISO 17665:2006, which outlines the requirements for moist heat sterilization processes in healthcare. It covers the validation, control, and monitoring of sterilization methods using saturated steam or water, ensuring safe and effective sterilization of medical devices. This standard is essential for maintaining product safety and compliance in the medical industry.

Anchor ISO 17665

Course Objectives

At the end of the program participants should be able to do the following:

  • Understand the philosophy and principles of sterilization.

  • Aware of validation and routine control of the moist heat sterilization method and requirement.

  • Understand the key factors for sterilization process development.

Course Outline

Set the State- Overview:


•    Ice breaker- Recognizing and Identifying STERILE              Product
•    Objectives of the workshop
•    Agenda
•    Administrative arrangement

​

Session 1: Overview of Sterilization


•    Introduction
•    Routine Process control

​

Session 2: Key Factor of Sterilization Process Development


•    Validation
•    Manufacturing environment
•    Bioburden and sterility test
 

Target Audience

This program is very useful to participants who handles and are actively involved in Quality especially those who are QA/QC Lab technician, and QA/QC Executive.

Duration

2 full-day courses running from 8.30 am to 5.30 pm. Physical Training (On-site).

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