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03 - 04 Feb 2021  • 

Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

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Estimated Turnout

100 - 500
Delegates
Based on previous editions

Editions

03 - 04 Feb 2021
+2 more editions

Frequency

Bi-annual
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Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers will educate you about various key elements of sterility .. Read more assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirements, Validation/Qualification, Operations, Environmental Monitoring Program requirements, Excursion investigations, DataTrending, Microbiological processes/methodology, Cleanroom cleaning/disinfection.

Mary

Mary

Lecturer at Federal University of Technology Minna, Niger state, Nigeria

Abuja, Nigeria
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