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Webinar on Lyophilization Technology

Event Details

Webinar on Lyophilization Technology

Time: November 10, 2015 from 10am to 11am
Location: Online
Street: 161 Mission Falls Lane, Suite 216
City/Town: Fremont
Website or Map: http://bit.ly/1RcUuDp
Phone: 18004479407
Event Type: webinar
Organized By: Adam Fleming
Latest Activity: Sep 29, 2015

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Event Description

Overview: 

Lyophilization cycles consist of three phases: Freezing, primary drying, and secondary drying. Conditions in the dryer are varied through the cycle to ensure that the resulting product has the desired physical and chemical properties and that the required stability and sterility is achieved and maintained.

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. Generating very large frozen particles due to the initial freezing process can cause the sedimentation rate to go way up causing a much longer cycle than effective design of the process can accomplish making the process more cost effective and higher quality. 

Why should you Attend: 

The fundamental principles and technology are coupled with practical aspects of lyophilization in the training program. Principles and concepts presented are later used to discuss real world pracdtical applications. The long term training sessions include participants in development, operations, engineering, technical services, quality, validation, and regulatory affairs. Brief on-line training addresses critical aspects of freeze drying to ensure compliance, validation and minimization of patient risk based on the development of the product proven to have been during the clinical trials before the product was transferred into commercial scale operations. 

Areas Covered in the Session:

  • Essentially a brief discussion about each of the Critical Aspects and related affects of Variables
  • Lyophilization 101 – Comprehension on each step of the Freeze Drying/Lyophilization Process
  • Understanding why various steps of the process become more advantageous and cost effective
  • Sublimation Rate Variability
  • Heat Transfer
  • Loss of Protein Activity
  • Freezing Affects on Primary Drying
  • Optimization of Primary Drying and Proof of the effectiveness of Secondary Drying
  • Effects of Freezing Method and Excipients on Protein Surface
  • Influence of Packing Density and the container selection
  • Residual Moisture Regulatory Considerations by the FDA

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. 

He has held permanent employee, temporary employee and company representative management positions with a multitude of the major pharmaceutical and biotechnology companies in the US. He has worked with or assisted more than two dozen companies with the establishment of controlled document/quality systems, FDA briefing and submittal documents, project management of several multimillion dollar projects including design, start-up and validation to assure fast track FDA approval by maintaining strict regulatory compliance.

Contact Detail:

NetZealous - Compliance4All,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.
Phone: +1-800-447-9407
Email: support@compliance4All.com
http://www.compliance4all.com/
Event Link : http://bit.ly/1RcUuDp

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