Reference book covers global sterilization issues
Quality, manufacturing, engineering and lab personnel have a new resource at their disposal that provides current information on international sterilization standards and practical guidance on how to incorporate them into the production process. Sterilization of Medical Devices includes chapters on ISO sterilization standards, validation, industrial sterilization methods, emerging sterilization technologies, support testing, manufacturing considerations for sterile devices, and reuse of devices.
The book was edited by Anne F. Booth, a quality GMP and sterilization specialist with more than 15 years` experience in medical device manufacturing; its content was excerpted from Booth`s newsletter, The Validation Consultant. To order, contact Interpharm Press, Inc (Buffalo Grove, IL) at (847) 459-8480. — TGW