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Upcoming Webinar on Microbial Testing in Sterilized Products

On May 28, 2025, CMC Research will host a crucial webinar titled "Practical Aspects and Validation Points of Microbial Testing in Sterilized Products and Sterile Pharmaceuticals". This event will commence at 13:00 JST and will be conducted via Zoom, complete with a recording for those unable to attend live. The session will be facilitated by Mr. Nozomi Ibara, the Quality Assurance Manager at Iwata Glass Industry Co., Ltd.

Event Details

The webinar aims to provide comprehensive insights into microbial testing methodologies and the necessary validation processes involved in the production of sterilized products and sterile pharmaceuticals. Participants can expect to gain:

• - An understanding of the environmental microorganisms and the fundamentals of microbial testing.
• - Insights into various microbial testing methods applicable to sterilized products and sterile pharmaceuticals.
• - Key validation points essential for conducting effective microbial testing.

Registration and Fees

The participation fee is set at 44,000 JPY (tax included), with discounted rates offered for subscribers of the CMC Research newsletter at 39,600 JPY and academic participants for 26,400 JPY. Each registration comes with supporting materials and access to the recorded session for those who miss the live presentation.

To register, please visit the CMC Research website for additional details and to secure your spot. Be sure to take advantage of the Q&A session during the webinar to clarify any uncertainties you may have regarding the topic.

Target Audience

This seminar is particularly beneficial for professionals in the pharmaceutical and medical device manufacturing sectors involved in:

• - The production, quality control, and quality assurance of sterile pharmaceuticals.
• - The manufacturing, quality management, and quality assurance of sterilized products.

Seminar Agenda

The webinar is structured as follows:
1. Basic Microbiology: Discussions will cover the classification and characteristics of microorganisms in the environment, sources of microbial contamination in manufacturing environments, and factors contributing to the growth of microbial contamination.
2. Overview of Microbial Testing: Participants will learn about the role of microbial testing, required equipment, reagents, consumables, and the step-by-step process of conducting microbial tests.
3. Practical Applications and Validation: A focus on the validation of microbial testing methods and specific applications such as sterility tests, microbial limits tests, endotoxin tests, and preservation efficacy tests will be explored.
4. Maintenance of Testing Infrastructure: Discussion on the evaluation and maintenance of equipment suitability, reagent preparation, the skill assessment of testers, and quality documentation.

About the Speaker

Mr. Nozomi Ibara has over two decades of experience in the field of microbial control and quality assurance. He has contributed significantly to the development of innovative solutions in microbial testing and management within the pharmaceutical industry. His expertise would greatly enhance the learning experience of the webinar attendees.

Don't miss the chance to expand your knowledge on this critical aspect of pharmaceutical manufacturing. Register today and ensure your understanding of microbial testing validation is up-to-date!

For further inquiries or assistance, feel free to reach out to CMC Research.

Note: Recording of the session will be available for review for a limited time after the live webinar. Recording or photographing during the event is strictly prohibited.