Validation of Sterilization Procedures and Usage of Biological Indicators in the Manufacture of Healthcare Products
スポンサーリンク
概要
- 論文の詳細を見る
Healthcare product manufacturers strive to provide safe, sterile products by validating and controlling manufacturing procedures. Validation study is the result of a multidisciplinary team effort. This successful effort relies on each discipline understanding the fundamentals of each technical disciplines and applying those fundamentals in terms of their own technical background. This paper is to introduce the basic concepts of sterilization methodology which are involved in validating various technical methods of sterilization and biological indicators (BIs). These will mainly address sterilization procedures in general terms and highlight on their microbiological aspects. The proper starting point is defining what sterility is and how it can be achieved through the validation studies by using BI.
- 日本防菌防黴学会の論文
- 2011-09-10
著者
関連論文
- Sterilization Efficiency of the Photocatalyst against Environmental Microorganisms in a Health Care Facility
- Relationship between the Contamination of the Nurse's Caps and Their Period of Use in Terms of Microorganism Numbers
- Validation of Sterilization Procedures and Usage of Biological Indicators in the Manufacture of Healthcare Products
- Modification of Polymer Surfaces of Medical Devices to Prevent Infections
- Confirmation of the Sterilization Effect Using a High Concentration of Ozone Gas for the Bio-Clean room
- Confirmation of the Sterilization Effect Using a High Concentration of Ozone Gas for the Bio-Cleanroom