Webinar Series: Contamination Control for Cell and Gene Therapy

Explore holistic steps to reduce risk and optimize processes in CGT operations

Webinar Series: Contamination Control for Cell and Gene Therapy

Explore holistic steps to reduce risk and optimize processes in CGT operations

Webinar Series: Contamination Control for Cell and Gene Therapy

Explore holistic steps to reduce risk and optimize processes in CGT operations

Webinar Series: Contamination Control for Cell and Gene Therapy

Explore holistic steps to reduce risk and optimize processes in CGT operations

Webinar Series: Contamination Control for Cell and Gene Therapy

Explore holistic steps to reduce risk and optimize processes in CGT operations



Cell and gene therapy (CGT) operations share the same contamination control requirements as the broader pharmaceutical industry, which utilizes current good manufacturing practices (cGMP). However, there are unique challenges.

Our four-part educational webinar series explores the heightened risks of contamination in CGT and provides holistic steps that you can take to reduce risk and optimize processes for your operation.

Learning Objectives

During this webinar series, you will:

  • Discover how to optimize operations while reducing risk
  • Understand processes and techniques to adapt an existing environment for CGT
  • Learn about the holistic approach to developing and maintaining your contamination control program
  • Find out how to simplify processes to reduce training time

Best Practices for Cell and Gene Therapy Manufacturing

It is vital to establish a robust contamination control program for your CGT manufacturing process to protect your products and increase speed to market. STERIS's best practices document discusses common challenges experienced in CGT manufacturing and how to address them.

Download Best Practices Document

Webinars

Cell and Gene Therapy Operations and Contamination Control Programs

Available On-Demand

The first webinar in our series takes a look at how to develop a contamination control program to address some of the more prominent CGT challenges. We provide an overview of cleaning and disinfection frameworks to accommodate speed to market, operate within existing environments, movement of materials and staff training. Finally, we review CGT case studies to share how others are successfully implementing a contamination control program.

Presenters: Daniel Klein – Senior Manager, Technical Services | Jim Polarine – Senior Manager, Technical Services

Watch the CGT Contamination Control Programs Recording Watch the CGT Operations Recording

Implementing VHP™ Biodecontamination in Cell and Gene Therapy Settings

Available On-Demand

This webinar introduces the basics of Vaporized Hydrogen Peroxide (VHP) and strategies to employ VHP as a decontamination method in aseptic manufacturing spaces for CGT operations. We review several VHP applications, including integrated, facility-wide, mobile and decontamination services.

Next, we offer guidance for choosing the appropriate deployment option for your CGT operation and explain the importance of combining VHP and manual cleaning for contamination control of aseptic spaces, including open cleanrooms, RABS, isolators and biosafety cabinets (BSCs). Lastly, we explore material movement best practices using VHP.

Presenters: Matt Hofacre – Senior Director, Technical Services | Juha Mattila – Director, Sterilization Technologies

Watch the CGT VHP Biodecontamination Recording Watch the CGT VHP Recording

Materials Movement and Contamination Control for Cell and Gene Therapy Operations

Available On-Demand

The third webinar in our series focuses on reducing the risk of materials becoming a transmission vector for microorganisms when they are transferred into an aseptic environment or staged for production activities.

We cover the development of mitigation measures, documentation and training strategies to reduce risk and improve productivity. We also review best practices for equipment preparation/wrapping, manual surface disinfection and disinfection using VHP pass-through chambers.

Presenters: Renee Buthe – Manager, Technical Services | Aaron Mertens – Senior Manager, Technical Services

Watch the CGT Materials Movement Recording Watch the Material Movement Recording

Cell and Gene Therapy Panel Discussion

Available On-Demand

Our final CGT webinar reviews and responds to frequently asked questions received throughout the first three webinars in the series. This interactive discussion features a panel of subject matter experts who will provide insight and advice to help you overcome challenges.

Presenters: Renee Buthe – Manager, Technical Services | Matt Hofacre – Senior Director, Technical Services | Daniel Klein – Senior Manager, Technical Services | Juha Mattila – Director, Sterilization Technologies | Aaron Mertens – Senior Manager, Technical Services | Jim Polarine – Senior Manager, Technical Services

Watch the CGT Panel Discussion Recording Watch the Panel Discussion Recording

Meet the Presenters

Renee Buthe, Technical Services Manager

Renee Buthe | Manager, Technical Services

Renee has over seven years of industry experience, specifically in cell and gene therapies. She has expertise in generating protocols for and performing environmental monitoring, airflow visualization studies and aseptic process simulations, reviewing batch records and authoring final reports. Renee holds a bachelor’s degree in biology.

At STERIS Life Sciences, Renee assists Customers with sterility assurance and sterility maintenance product applications.

Renee is currently an instructor through the Parenteral Drug Association (PDA) training institute and an active member of the association.


Matt Hofacre, Director of Application Project Management

Matt Hofacre | Senior Director, Technical Services

Matt has over two decades of experience in pharmaceutical and biopharmaceutical production, advanced therapy medicinal product production, high containment, food and beverage, medical device and laboratory research industries. He holds a master’s degree in finance and marketing and a bachelor’s degree in chemical engineering.

For STERIS Life Sciences, Matt supports Customers globally with design applications, project maintenance and technical guidance for integrated Vaporized Hydrogen Peroxide (VHP), steam sterilization, washing, pure steam, water systems and services. He is a student of lean practices to maximize value stream to Customers.

The Parenteral Drug Association (PDA), the International Society for Pharmaceutical Engineering (ISPE) and the American Society of Mechanical Engineers (ASME) have welcomed Matt as a presenter and trainer at several national and international conferences.

Matt co-authored “PDA Technical Report No. 48 Moist Heat Sterilization Systems: Design, Commissioning, Operation, Qualification and Maintenance” and has contributed to numerous other articles on water for injection systems, VHP and pharmaceutical equipment selection.


Dan Klein, Senior Manager, Technical Services

Daniel Klein | Senior Manager, Technical Services

Dan has over two decades of industry experience, including working in research and development for microbiology and clinical affairs. He has also managed a contract testing laboratory. Dan holds a master’s degree in biology and a bachelor’s degree in microbiology.

At STERIS Life Sciences, Dan provides technical expertise to Customers and helps troubleshoot and solve contamination issues. He supports Customers with a variety of critical processes and general understanding of the latest developments in the industry. He frequently presents data and other information at international industry meetings and sponsored events.

Dan is an active member of ASTM International, the Association for the Advancement of Medical Instrumentation (AAMI), the Parenteral Drug Association (PDA), the Association of Official Analytical Collaboration (AOAC) International, the Institute of Environmental Sciences and Technology (IEST) and the Center for Biofilm Engineering (CBE). He previously served as Chairperson of the AOAC International’s Committee on Antimicrobial Efficacy Testing. He is an active participant in ASTM’s E35.15, E55.08 and D37 Committees and a primary member of AAMI Work Group 08.

Throughout his professional experience, Dan has authored numerous industry articles and book chapters in peer-reviewed journals related to disinfection and sterilization.


Juha Mattila, Director, Sterilization Technologies

Juha Mattila | Director, Sterilization Technologies

Juha has over two decades of experience in pharmaceutical, research and biosafety technologies. He manages the STERIS Life Sciences portfolio of products for Vaporized Hydrogen Peroxide (VHP) and steam sterilization, material transfer biodecontamination technologies and water for injection and pure steam generation systems. He holds a master’s degree in business informatics and a bachelor’s degree in heating, ventilation and air conditioning (HVAC) and process engineering.

In addition to being an active member of the Parenteral Drug Association (PDA), the International Society for Pharmaceutical Engineering (ISPE) and the Finnish Biosafety Network, Juha has authored several technical articles and spoken at many industry events. He also contributes to the International Organization for Standardization (ISO), the European Committee for Standardization (CEN) and the British Standards Institution (BSI) work groups considering these technologies.

Juha provided commentary through the PDA for the European Union (EU) Good Manufacturing Practices (GMP) Annex 1 draft and participated in the PDA EU GMP Annex 1 Workshop.


Aaron Mertens, Senior Technical Services Manager

Aaron Mertens | Senior Manager, Technical Services

Aaron has over two decades of experience in pharmaceutical manufacturing, with expertise in cleaning, disinfection, sterilization and contamination control. He has held several positions within the pharmaceutical industry, with experience working at pharmaceutical manufacturing organizations representing quality assurance programs and working with global industry regulatory agencies. He holds a bachelor’s degree in genetics.

At STERIS Life Sciences, Aaron performs global manufacturing site evaluations and consultations to ensure compliance with international regulations. He is also responsible for providing global technical support for critical environments, sterility assurance and sterility maintenance application and validation.

Aaron is an active member of the Parenteral Drug Association (PDA) and the International Society for Pharmaceutical Engineering (ISPE). He previously served as President of the ISPE Great Lakes Chapter and is currently on the chapter’s Board of Directors. He is also a member of the ISPE Sterile Products Processing Steering Committee.

Additional professional activities for Aaron include delivering technical content to the industry with posters, publications, virtual and live technical presentations, as well as leading global sterilization master classes.


Jim Polarine, Senior Technical Services Manager

Jim Polarine | Senior Manager, Technical Services

Jim has three decades of experience in cleaning, disinfection, microbial excursions and disinfectant validation and testing. He holds a master’s degree in biology.

Prior to joining STERIS Life Sciences, Jim worked as a Clinical Research Manager with the Department of Veterans Affairs in St. Louis, MO and as a biology and microbiology instructor at the University of Illinois.

A member of STERIS Life Sciences team for the past 23 years, Jim’s current technical focus is on microbial control in cleanrooms and other critical environments. He conducts on-site training, webinars and high-level technical support for Customers in the biopharmaceutical industry.

As a 2019 Parenteral Drug Association (PDA) Michael S. Korczynski Award recipient, Jim was recognized for his contributions toward the development of PDA's international activities. He has given lectures around the globe on issues related to cleaning and disinfection, microbial control in cleanrooms and validation of disinfectants. He has also published several PDA book chapters and articles related to cleaning, disinfection and contamination control.

Jim currently serves as President of the PDA Missouri Valley Chapter and Technical Coordinator for the Institute of Environmental Sciences and Technology (IEST). He is also the current Membership Vice President of the IEST Executive Board. He is an active member of the International Society for Pharmaceutical Engineering (ISPE), the American Society for Microbiology (ASM), the Society for Industrial Microbiology and Biotechnology (SIMB) and other industry associations.