This course will detail various sterilization methods and various approaches for the validation of a sterilization process.
Why Should You Attend:
Since there are so many different interpretations of regulatory statements and because different agencies have different philosophies, and there are those who need a deeper comprehension of the sterilization design relative to microbiological impact, this course will:
Discuss the definition of ‘sterile’
Elaborate how to get there by describing different sterilization methods
Discuss various approaches for the validation of a sterilization process using moist heat as template
Who Will Benefit:
Manufacturing operations personnel
QA/QC professionals
Formulation ,product and process development personnel
Regulatory affairs professionals
Research and development personnel
Sterility assurance team members
Instructor Profile:
Jerry Dalfors has over 40 years of business administration, consultative, technical and managerial experience in the development and manufacture of highly regulated biopharmaceutical products including injectables, biologics, medical devices, and oral dosages. He has held various management positions with several major pharmaceutical and biotechnology companies in the US.
Note:
Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.
For Registration:
http://www.complianceonline.com/methods-of-terminal-sterilization-and-probability-of-survival-approach-vs-overkill-approach-webinar-training-703633-prdw?channel=sciencedz