Unsere Homepage in englischer Sprache:

http://www.microbiological-evaluation-of-sterile-barrier-systems.com/ 

Universitätsmedizin Göttingen

Prof. Dr. med. Hartmut Dunkelberg

Dr. med. U. Schmelz

Literatur

Dunkelberg H, Wedekind S. A new method for testing the effectiveness of the microbial barrier properties of packaging materials for sterile products. Biomed Tech (Berl) 2002;47:278-284
 
Dunkelberg H, Wedekind S. Preliminary results for a new final package test to assess the quality of sterile package systems. Infect Control Hosp Epidemiol 2004; 25: 26-29
 
Dunkelberg H, Rohmann S. Test to determine sterile integrity of wrapped medical products at a probability of recontamination of 1:1 000000. Infect Control Hosp Epidemiol 2006; 27: 367-371
 
Dunkelberg H, Fleitmann-Glende F. Measurement of the microbial barrier effectiveness of sterilization containers in terms of the log reduction value for prevention of nosocomial infections. Am J Infect Control 2006;34:285-9
 
Dunkelberg H., Schmelz U. Sterilbarrieresysteme für Medizinprodukte. In Kramer A., Assadian O. (Hrsg) Wallhäußers Praxis der Sterilisation, Desinfektion, Antiseptik und Konservierung. Thieme 2008  
 
Dunkelberg H., Schmelz U. Determination of the efficacy of sterile barrier systems against microbial challenges during transport and storage. Infect Control Hosp Epidemiol 2009;30:179-183

Dunkelberg H. Sterile supply of medical devices and pharmaceutical products - quality standards and applied risk management. Pharm Ind 2016;78:1644-1648

Dunkelberg H. Aufrechterhaltung der Sterilität von Sterilgütern in der Poststerilisationsphase. Anästh Intensivmed 2012;53:S234

Hartmut Dunkelberg: On-site application of the exposure chamber method in hospitals to control the airborne microbial recontamination of sterilised products during shelf life. Congress of the German Society for Hygiene and Microbiology, Hamburg, September 30 to October 4, 2012   

Dunkelberg, H.: From a time- or event-related to a data-based shelf-life practice for sterilized items. 14th World Sterilization Congress & 8th National Sterilization Disinfection Congress of Turkey, 6-9 November 2013, Antalya, Turkey

Dunkelberg, H.: Requirements of validation of packaging systems and sterility assurance. 16th World Sterilization Congress & Annual Conference of AFS, 7-10 October 2015, Lille, France

Dunkelberg, H.: Quality standards and applied risk management in sterile supply of medical devices and pharmaceutical products. 1st European Lab Technology Forum 2015, November 5-6, 2015, Sartorius College, Goettingen, Germany 

Lectures and presentations 2015-2017:

Dunkelberg H. Requirements of validation of packaging systems and sterility assurance. 16th World Sterililization Congress & Annual Conference of AFS, 7-10 October 2015 Lille, France 

Dunkelberg H. Quality standards and applied risk management in sterile supply of medical devices and pharmaceutical products. 1st European Lab Technology Forum 2015, November 5-6, 2015, Sartorius College, Goettingen, Germany  

Dunkelberg H. Assessment of compatibility of microbial barrier properties of packaging material of terminally sterilized products with the airborne microbial challange during the storage period (Abstract). VAAM Annual Meeting 2017, 69th Annual Meeting of the DGHM, 5-8 March 2017, Wuerzburg, Germany

Dunkelberg H. Evidence based sterile storage. 10th International Sterilization  Disinfection Congress, 29 November - 3 December 2017, Antalya, Turkey

Dunkelberg H. Proposal for controlling the maintenance of sterility at the highest possible sterility assurance level up to the point of use. 18th World Sterilization Congress, Bonn, 4-7  October, 2017