Guide to FDA Requirements and Importance of Medical Device Calibration
Engineers Design Color- Changing Compression Bandage
Improved 3D Printing for Patient-Specific Medical Diagnosis
Data, Data Everywhere: Why the Medical Device Industry Must Embrace the Fourth Industrial Revolution
Implantable Islet Cells Come with Their Own Oxygen Supply
Evaluating Electronics Contract Manufacturers for Medical Devices
Two-Component Molding Can Solve Medical Design Challenges and Reduce Costs
Therapeutic Gel Shows Promise Against Cancerous Tumors
Scientists Develop Elastic Metal Rods to Treat Scoliosis
Key Factors for Choosing Silicone Solutions in Medical Device Lubrication
On Demand Webinars

The global regulatory landscape around Ethylene Oxide (EO) residues is a topic of increasing interest.

This webinar will provide:

  • An overview of EO sterilization
  • The status of ISO standard 10993-7:2008, which serves as an international authoritative document for medical device manufacturers. The following topics will be covered:
    • Testing according to product category and product use
    • Concomitant EO exposure
    • Topical contact
    • Special product categories (intraocular lenses, blood oxygenators etc.)
    • Test method and validation
    • ISO 10993-7 revision for products intended for neonates and children /recomendation by ANSM – French Regulator
    • Fugitive EO emission from EO treated products must be monitored throughout the supply chain to safeguard minimum worker exposure.
    • Legislation regarding EO emissions in the supply chain will also be addressed.

An audience Q&A follows the live presentation.


Dr. Stefan Reisbacher, SteriPro Consultant, Sterigenics

Click here to view webinar