Sterilization Of Medical Devices Training Course Scheduled For October 1516, 2026, Covering Regulatory Requirements, Standards And Sterilization Processes
Dublin, Sept. 16, 2026 (GLOBE NEWSWIRE) -- "Sterilization of Medical Devices Training Course (Oct 15th - Oct 16th, 2026)" has been added to ResearchAndMarkets.com's offering.
The Sterilization of Medical Devices Training Course, delivered by IPI Academy, will take place as an online event on October 15–16, 2026, providing two days of training on medical device sterilization, regulatory requirements, supporting standards and the science behind processes used to achieve and maintain sterility. The course is designed for professionals involved in sterilization, microbiology, quality management and regulatory compliance.
Key Event Facts
Course: Sterilization of Medical Devices Training Course
Date: October 15–16, 2026
Format: Online event
Duration: 2 days
Focus: Medical device sterilization, regulatory requirements and supporting standards
Sterilization is identified on the course page as a key process in producing sterile medical devices. The training examines requirements relating to devices supplied or intended for use in a sterile state, including general safety and performance considerations, independent third-party conformity assessment and evidence of successful sterilization. It also addresses standards covering designation of products as sterile, validation and routine control of sterilization processes, and maintaining sterility through appropriate sterile barrier systems.
Why You Should Attend
- Examine the role and portfolio of sterilization standards, including their interaction with medical device regulations. Explore ISO 14937 and common features of validation and routine control. Review microbiology topics including contamination control, bioburden estimation and tests of sterility. Study radiation, ethylene oxide and moist heat sterilization requirements, including relevant EN ISO standards. Apply course concepts through syndicate exercises covering radiation sterilization and ethylene oxide sterilization, followed by feedback and discussion.
The course provides professionals with a structured opportunity to understand regulatory requirements for sterilization and how they relate to the supporting standards and technical processes used in medical devices. The programme also covers microbial inactivation, sterility assurance, biological indicators, sterilization dose establishment and Installation Qualification, Operational Qualification and Performance Qualification.
Who Should Attend
- The course is intended for microbiologists and sterilization professionals, Quality Management System (QMS) specialists, Regulatory Compliance specialists, Internal Auditors, and Regulatory and Quality professionals.
Featured Course Provider
Annette Callaghan, Sterile Management Systems, is the named course provider. She is a quality management professional, chartered biologist and member of the Royal Society of Biology, with more than 35 years' experience across the medical device, pharmaceutical, biotechnology and food industries. She is also a Qualified Notified Body Lead Auditor and has been eligible to act as a Qualified Person under Directive 2001/83/EC, as amended, since 1993.
With the online course scheduled for October 15–16, 2026, professionals responsible for sterilization, regulatory compliance, quality systems, microbiology and auditing can review the programme and register their interest through Research and Markets.
For more information about this training visit
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