Aseptic Processing Overview and Validation 2019

Aseptic Processing Overview and Validation


This course will provide an overview of the requirements for aseptic

and bulk manufacturing operations, including facility design,

contamination controls and acceptable personnel behaviors.

Why should you Attend:
Explain the difference between Aseptic and Bulk processing
Understand facility and personnel requirements necessary to maintain

microbial control
Explain basic principles of microbiology and microorganism recovery

in relation to cleanroom environmental monitoring (EM) and impact to

Understand the gowning requirements associated with different

cleanroom classifications

Areas Covered in the Session:
Review Clean Area Behaviors
Personnel gowning requirements
Good clean area behaviors/practices
Practices to avoid – and why

Who Will Benefit:
Engineering & Validation
Facilities / Maintenance
Quality Assurance
Regulatory Affairs

Speaker Profile:
Kelly Thomas has over two decades of cGMP hands-on industry

experience in both pharmaceutical and medical device manufacturing

operations. Her experience covers all Quality Systems; as well as, all

areas of validation; including, process/product validation, facilities

validation, CSV and 21 CFR Part 11, test method validation,

equipment/automated processes and cleaning validation.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com

Ad Reference ID: 8285c109778c5f82

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