Sterile Filtration of Pharmaceutical Products - What you need to know to meet Validation and Regulatory Requirements

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Category Pharmaceutical

Deadline: February 16, 2016 | Date: February 16, 2016

Venue/Country: Online, U.S.A

Updated: 2016-02-06 19:41:18 (GMT+9)

Call For Papers - CFP

Sterile filtration is one of the most critical steps in sterile pharmaceutical manufacture. This is because the filtration process provides the assurance of sterility in the finished drug product.

Therefore, the design, validation and ongoing monitoring of a sterile filtration system is essential for assuring the quality and safety of the pharmaceutical product.

Proper understanding and testing of the sterile filtration system according to international regulatory standards is important for both the validation and ongoing monitoring of the system.

Why you should attend:

It is important that the sterile filtration process is fully understood and properly validated for your particular application. The process requirements and validation needs differ based on the filtration requirement. This webinar will give you a comprehensive understanding of this important subject with an emphasis on the different types of sterilizing filtration available and their application to your particular system. For example, the application of sterile filtration to use-point compressed air is discussed in detail.

A review of the different filtration media is provided with the construction characteristics and properties of each detailed. A detailed description of a typical pharmaceutical sterile filtration system with its individual components is provided. Engineering schematics are included. Microbiology and particle retention mechanisms are discussed.

Integrity testing methods are detailed as well as media qualification. Procedures for the sterilization of the filter are presented (SIP, autoclave, etc.).

The proper validation of sterile filtration is important to ensure that the filter will reproducibly remove undesirable components (bio-burden) while allowing passage of desirable components (drug product). The operating parameters of time, pressure and temperature are fully discussed as well as the filters potential effect on the product (compatibility, leachable, fibers, endotoxin, etc.). Microbial retention challenge testing is one of the validation requirements.

Finally, a compilation of all FDA/EU GMP regulatory guidances concerning sterile filtration are presented. Related to this; the responsibilities of the filter manufacturer vs. the filter user is fully discussed.

Areas Covered In the Seminar:

Sterile filtration - Importance of Quality

Sterility Assurance of Sterile Filtration

Sterile Filtration System Design

Discussion of Different Filtration Media Properties and Retention Mechanisms

Methods for Sterilization of Filters

Validation of Sterile Filter Systems

Microbial Retention Challenge Testing

Integrity Testing

Product Compatibility Testing

Extractable/Leachable Testing

Regulatory Requirements

Who will benefit:

This webinar will provide valuable assistance to all personnel in:

Quality Assurance

Environmental Monitoring

Microbiology

Manufacturing

Validation

Engineering

Maintenance

Webinar includes:

Q/A Session with the Expert to ask your question

PDF print only copy of PowerPoint slides

60 Minutes Live Presentation

Certificate of attendance