Transforming endotoxin testing: Experiences with rFC and automation

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Tuesday, 29 September 2026

Europe and Asia Pacific
9:00 AM CEST | 12:30 PM IST | 3:00 PM CST | 4:00 PM JST | 5:00 PM AEST

Americas and Europe
8:00 AM PDT | 11:00 AM EDT | 4:00 PM BST | 5:00 PM CEST 


Join Dr. Harmen Hawer for a practical discussion on the transition to more sustainable endotoxin testing approaches and the journey from manual processes to automated endotoxin testing. Drawing on real-world experience, Dr. Hawer will compare traditional endotoxin testing methods with modern, sustainable alternatives and discuss key considerations for automating laboratory workflows to improve efficiency, consistency, and data integrity.

Attendees will gain: 
Insights into laboratory workflows, implementation challenges, lessons learned during the transition to non-animal-derived reagents, and practical considerations for successfully introducing automated endotoxin testing into the QC laboratory.

Who should attend:
This webinar is ideal for scientists, analysts, and leaders in QC microbiology, pharma and biopharma manufacturing, biotechnology, cell and gene therapy, and CDMOs evaluating recombinant technologies.

The webinar includes a Q&A session and will last approximately 60 minutes.
Unable to attend? Register now and receive an email notification as soon as the event is available for on-demand viewing.

We look forward to welcoming you,
Your Lonza Bioscience Team

Speakers

Speaker
Dr. Harmen Hawer
Pharma Consultant & Project Lead
Hawer Consulting
Moderator
Dr. Thomas Winkler
Director, Subject Matter Experts, EMEA
Lonza
Role:
First Name Last Name
Job Title
Company

Speakers

Speaker
Dr. Harmen Hawer
Pharma Consultant & Project Lead
Hawer Consulting

Dr. Harmen Hawer is Head of the Microbiological Laboratory at Panpharma and founder of Hawer-Consulting, a firm providing scientific, quality, GMP, and project support to the biopharmaceutical industry.
He specializes in sterile manufacturing, pharmaceutical microbiology, hygiene, and pharmaceutical water systems, quality management, GMP, and modern QC methods.
He supports biopharmaceutical companies through strategic consulting, project leadership, qualification and validation activities, and international training programs.
Moderator
Dr. Thomas Winkler
Director, Subject Matter Experts, EMEA
Lonza

Tuesday, 29 September 2026

Europe and Asia Pacific
9:00 AM CEST | 12:30 PM IST | 3:00 PM CST | 4:00 PM JST | 5:00 PM AEST

Americas and Europe
8:00 AM PDT | 11:00 AM EDT | 4:00 PM BST | 5:00 PM CEST 


Join Dr. Harmen Hawer for a practical discussion on the transition to more sustainable endotoxin testing approaches and the journey from manual processes to automated endotoxin testing. Drawing on real-world experience, Dr. Hawer will compare traditional endotoxin testing methods with modern, sustainable alternatives and discuss key considerations for automating laboratory workflows to improve efficiency, consistency, and data integrity.

Attendees will gain: 
Insights into laboratory workflows, implementation challenges, lessons learned during the transition to non-animal-derived reagents, and practical considerations for successfully introducing automated endotoxin testing into the QC laboratory.

Who should attend:
This webinar is ideal for scientists, analysts, and leaders in QC microbiology, pharma and biopharma manufacturing, biotechnology, cell and gene therapy, and CDMOs evaluating recombinant technologies.

The webinar includes a Q&A session and will last approximately 60 minutes.
Unable to attend? Register now and receive an email notification as soon as the event is available for on-demand viewing.

We look forward to welcoming you,
Your Lonza Bioscience Team
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Speakers

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Speaker
Dr. Harmen Hawer
Pharma Consultant & Project Lead
Hawer Consulting
Moderator
Dr. Thomas Winkler
Director, Subject Matter Experts, EMEA
Lonza
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Speaker
Dr. Harmen Hawer
Pharma Consultant & Project Lead
Hawer Consulting
Moderator
Dr. Thomas Winkler
Director, Subject Matter Experts, EMEA
Lonza
Role:
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Job Title
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