For more information about this or any other on-site seminar, contact your STERIS Account Manager or call 1-314-290-4743.
Meet regulatory requirements and validate process equipment faster
Your team will learn cleaning and cleaning validation best practices to ensure that your cleaning process removes chemical and microbial residues from product contact surfaces of process equipment.
This seminar also teaches practical aspects of meeting global regulatory requirements.
A 2-day, onsite cleaning validation training course for up to 50 employees of a company in the pharmaceutical manufacturing industry.
Seminar Curriculum
Monitoring Issues Troubleshooting Cleaning Problems
Attendee Experience Level Introductory to Intermediate
Cost $5,000(USD), plus travel expenses for trainers
What's Included? Seminar and notes for up to 50 attendees
Register your pharmaceutical manufacturing company for this comprehensive two-day cleaning validation training course.
A team of experts from the STERIS Technical Service group will lead the cleaning validation seminar. The trainers have in-depth experience from working in pharmaceutical manufacturing. They travel the world sharing their knowledge of cleaning validation at major events for industry leaders, such as the Parenteral Drug Association (PDA) and International Society for Pharmaceutical Engineering (ISPE).
Many pharmaceutical manufacturers train employees using this course, but each seminar is tailor-made. The cleaning validation seminar is adapted for your specific company and business needs as well as your country or geographic region. And while this course is designed for introductory to intermediate level, it can be personalized for the experience level of your team.
Get the latest pharmaceutical manufacturing information on everything from cleaning and validation to decontamination and sterilization.
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