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Aseptic process simulations resources

Learn more about media fills for aseptic process simulations, including an overview of our cold filterable media range and flexible bioprocess container formats, as well as scientific webinars straight from industry experts. 

Webinars

Webinar series: The art of the aseptic simulation

 

Part I - Designing for optimal contamination detection

In this webinar, our expert speaker will discuss aseptic process simulations (APS), a critical component of sterility assurance. Topics include modern APS design principles, how to align simulations with actual production risks, selecting the right culture media for your APS and growth promotion testing.

 

Part II - Inspecting, interpreting, and integrating APS results

In part II of our APS webinar series, our expert speaker examines how to evaluate, interpret, and integrate APS results to provide meaningful evidence of process capability, strengthen sterility assurance, and reinforce your site’s overall Contamination Control Strategy (CCS).

Speaker:

Vanessa Vasadi Figueroa, Chief Executive Microbiologist and Independent Consultant at VVF Science®

Aseptic Process Validation – A risk-based approach webinar

In this webinar, we will discuss the principles of aseptic process validation based on current regulatory expectations and industry best practices, and evidenced via supporting case studies. Plus, hear more about the risk assessment approach and critical success factors for effective media fill simulations.

Speakers:

Shanshan Liu, Technical Director at No Deviation

Laura Noone, Senior Engineer and Sterility Assurance Technical Lead at No Deviation

Environmental monitoring and media fills: Theory and practical

A two-part webinar series dedicated to the theoretical and practical approach to Environmental Monitoring and Media Fill in pharma and biopharma companies.

Speaker: Dr. Tarun Chugh, Ph.D., Microbiology

SIMco Pharma Consultancy

Brochures and literature

Media Fills product overview

Take a look at our Media Fills Product Overview to learn more about how our high quality Thermo Scientific cold filterable media can ensure smooth validation of your aseptic processes.

  Brochure: Environmental monitoring solutions

Optimize your contamination control strategy to ensure product quality and patient safety with our range of environmental monitoring solutions. 

Whitepaper: From Design to Validation: Implementing Microbiological Control Strategies for New Sterile Environments

As biologics manufacturing grows, maintaining sterility and regulatory compliance has become increasingly complex. This whitepaper explores key considerations for developing and validating contamination control strategies, including risk-based monitoring, critical control point identification, environmental monitoring best practices, process qualification, and data-driven contamination control.

Featured video

Customer testimonials

APS media fill customer testimonial by Kedrion Biopharma

 

Discover how Kedrion uses Thermo Scientific APS media fill products in its aseptic process simulation activities. This article highlights Kedrion’s experience using our solutions and explores how Thermo Fisher Scientific helps support robust, reliable media fill workflows for pharmaceutical manufacturing.

For Laboratory Use Only. Not for use in diagnostic procedures.