
Emil Laske
22 October 2026
Understanding Cleanroom Manufacturing for Medical Devices
4-hour
Cleanroom design and operation, cleanroom classification and testing, microbiological monitoring, additional considerations (chemical contamination / aseptic processing), detailed review of ISO 14644 parts 1-5 and EN 17141:2020, overview of ISO 14644 parts 7-10, ISO 14698 parts 1-2 and ISO 11737-1 as well as EU GMP
Annette Callaghan
EL
Issued to
Emil Laske
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Credential Verification
Issue date: October 22, 2026
ID: f942da91-7689-4e1e-b35a-b4031df28e56
Type
Course
Level
Professional
Price
Paid
Earning Criteria
Participation
Attended the course held by Educo Life Sciences.
Watching
Or watched the recorded materials for the course held by Educo.