Monday, 18. March 2019, San Diego CA, Aseptic Processing Overview and Validation 2 Days Workshop

Aseptic Processing Overview and Validation 2 Days Workshop
Location :18-19 March , 2019 San Diego CA
Course “Aseptic Processing Overview and Validation 2 Days Workshop “ has been Pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.

"Each attendee will receive 2-Day workshop materials by the speaker. Seminar Also Includes Certificate, Complimentary Breakfast, Lunch & High Tea/Coffee provided by WCS"

Overview
This course will provide an overview of the requirements for aseptic and bulk manufacturing operations, including facility design, contamination controls and acceptable personnel behaviors. Cleanroom classifications and the techniques for proper cleaning and disinfection are presented; along with a high-level overview of microbiology in regards to cleanroom environmental monitoring and the associated impact to product and patient health and safety. This course will also review the guidance provided in USP to ensure compliance with regulatory expectations are met.

Course Objectives
At the completion of this course, attendees will be able to:• 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 product• Understand the gowning requirements associated with different cleanroom classifications• Explain basic principles of aseptic processing, including:o Cleanliness classificationso Process differences between aseptically produced and terminally sterilized product
o Relation of manufacturing and handling procedures to sources of product contaminationo The differences between cleaning, disinfection and sanitizationo Proper cleaning / disinfectant techniqueo Elements of a robust environmental program and why EM is importanto The role of isolator technology• The purpose of media fills, and elements critical to their success• Identify behaviors that are or are not appropriate when working in controlled areas, and why• Identify ways that they can impact/improve site-specific EM and aseptic behavior issues

Session Highlights
Topic 1: Basic Micro Review
• The role of environmental monitoring• Types & sources of microorganisms• The impact of microorganisms on product and patient health and safety
Topic 2: Review Aseptic Processing Basics
• Cleanliness classifications• Process differences between aseptically produced and terminally sterilized product• Relation of manufacturing and handling procedures to sources of product contamination• The differences between and the purposes of cleaning, disinfection and sanitization• Proper cleaning techniques• The role of isolator technology
Topic 3: Review Clean Area Behaviors • Personnel gowning requirements• Good clean area behaviors/practices• Practices to avoid – and why• Review site-specific EM/aseptic behavior observations/risks & ask attendees to brainstorm ways to change/improve/eliminate these behaviors & risks
Topic 4: Aseptic Validation
• The purpose of media fills, and elements critical to their success • Target Audience: Operations employees who are required to enter controlled environments as part of their job function – includes some or all of the employees in the following departments:o Productiono QC Microo Engineering & Validationo Facilities / Maintenanceo Quality Assurance

Who will benefit
Operations employees who are required to enter controlled environments as part of their job function – includes some or all of the employees in the following departments:o Productiono QC Microo Engineering & Validationo Facilities / Maintenance
Instructor Profile


Ms. 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.
Utilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.

If you have problems registering or have registration questions: email us support@ call us Toll Free 844-267-7299
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