Sterile Filtration of Pharmaceutical Products - Validation and Regulatory Requirements

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.

Why Should You Attend:

This course will offer a broad review of:

Different filtration media with the construction characteristics and properties of each detailed

A typical pharmaceutical sterile filtration system with its individual components

Engineering schematics

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

Quality Assurance

Environmental Monitoring

Microbiology

Manufacturing

Instructor Profile:

Roger Cowan is the founder and owner of R Cowan Consulting Services LLC, a consulting company specializing primarily in the area of pharmaceutical contract manufacturing. He has 35 years' experience in pharmaceutical quality assurance and manufacturing. In his career, Mr Cowan has held various manager / director positions in quality assurance, QC laboratory, technical services validation, manufacturing, and clinical supply manufacturing and distribution. He has taught courses in microbiology at Seneca College (pharmaceutical technology program) in Toronto, Canada.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/understanding-requirements-of-life-safety-code-in-esrd-webinar-training-703727-prdw?channel=sciencedz