1. International Organization for Standardization, 2016. ‘Medical devices - Quality management systems - Requirements for regulatory purposes’ (ISO 13485:2016).
2. International Organization for Standardization, 2009. ‘Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices’ (ISO 143927:2009).
3. W.A. Rutala and D.J. Weber, ‘Guideline for disinfection and sterilization in healthcare facilities, 2008′, 2008.
4. Effect of gas-plasma sterilization on the osteoinductive capacity of demineralized bone matrix;Ferreira;Clin. Orthop.,2001
5. Sterilization and virus inactivation by supercritical fluids (a review);Perrut;J. Supercrit. Fluids,2012