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Lyophilization 2017 - Lyophilization Technology effective design of the process

Date2017-03-23

Deadline2017-03-22

VenueFremont, USA - United States USA - United States

KeywordsRegulatory requirements; Roles of Validation Engineer; FDA Regulations Training

Websitehttp://www.compliance4all.com/control/w_...

Topics/Call fo Papers

Overview:
During the freezing phase, the goal is to freeze the mobile water of the
product. Significant supercooling may be encountered, so the product
temperature may have to be much lower that the actual freezing point of
the solution before freezing occurs.
Why should you Attend:
The fundamental principles and technology are coupled with practical
aspects of lyophilization in the training program. The long term training
sessions include participants in development, operations, engineering,
technical services, quality, validation, and regulatory affairs.
Areas Covered in the Session:
Sublimation Rate Variability
Heat Transfer
Loss of Protein Activity
Freezing Affects on Primary Drying
Who Will Benefit:
Compliance Manager
Process Engineer
Validation Manager
Regulatory Manager
Speaker Profile:
Jerry Dalfors has extensive (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.
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com

Last modified: 2017-01-03 18:35:27