23.04.2016

Good Manufacturing Practice (GMP) and Sterile Applications Knowhow Transfer from Pharmaceutical Operations to Stem Cell Laboratories

For Good Manufacturing Practice (GMP) and Sterile Applications Knowhow Transfer from Pharmaceutical Operations to Stem Cell Laboratories will be made to share information on the following heading ; Stem Cell Application Laboratory design requirements, Design Criteria of Cleanroom  Behaving and the Operational Rules for the Sterile Area Cleaning and Disinfection Applications for...

DEVAMINI OKU
23.04.2016

ISO 14644-1:2015Cleanroom Standard “What’s New?”

ISO 14644-:2015 just published as of end of 2015 by Technical Committee 209. This interactive presentation wil cover new, changed and developed parts and its effects in the field. 

DEVAMINI OKU
23.04.2016

Risk Based Approach Cleanrooms and Controlled Environments

Today, almost every kind of cleanroom process is carried out by risk based evaluation. More than classical written-formats, risk based approach has its own aspects such as different risk factors and process dynamics. This also causes uncertainity and grey areas in application. Different than concentional approach, lets have a look at this multidisciplinary process together in the light of...

DEVAMINI OKU
01.02.2016

International Cleanroom Education Board

Below you can find the list of courses presently held by the International Cleanroom Education Board. Please send us a message if you want to register to one of our courses. You can also visit each society's website for more information about indvidual courses and schedule. Name Society Field Type Cleanroom Basic...

DEVAMINI OKU