Endoscope manufacturers and healthcare facilities are under increased scrutiny from regulatory bodies, including the US FDA. It is essential that both manufacturers and end users understand the increasing requirements enacted to improve patient safety.

This webinar covers the important changes enacted in industry standards and guidance documents relating to the reprocessing of endoscopes in health care facilities and the validation methods used to generate the reprocessing instructions.

Attendees will learn:

• Upcoming and enacted changes to key industry standards and guidance documents
• Reasons for the changes to these documents
• Explanation of the recommendation at the national level to move towards terminal sterilization