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

Expired
Dates : 18 June 2020 » 19 June 2020

Place : Dallas, Texas
United States

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Organizer : Complianceonline

Topic : Health and Medicine; Pharmacology and Drug Development
Engineering and Technology;
Keywords: Design, Manufacturing
Description :

This course will educate you about various key elements of sterility 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. The types of micro-organisms, typical mitigation steps in ensuring an effective contamination control through Personnel Training (Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures),Gowning Controls, Personnel Training, Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training (Entry and Exit Policy), Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program and the Basics of Sterilization Processes- Physical and Chemical Processes will also be discussed. The various regulatory bodies’ requirements such as 21 CFR Part 211 (mostly relevant 211.113 “Control of microbiological contamination”, ISO 14644 (Various Parts), FDA Guidance for Industry: Sterile Drug Products Produced By Aseptic Processing - Current Good Manufacturing Practice”) amongst others and the criticality of aseptic processing and other key contamination control evaluators during the manufacture and testing of products are important to the quality determination and release of the finished manufactured products.

Topics: Cleanroom regulations, Cleanroom classifications, Cleanroom design considerations, Cleanroom qualification, Cleanroom cleaning validation IOQ/PQ, Cleanroom Routine Monitoring and Excursion Investigation, Cleanroom Environmental Monitoring Program, Environmental Monitoring Program, Cleanroom Monitoring, Excursion Investigation and Trending of Data, Cleanroom Personnel Training, Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures, Cleanroom Trafficking, Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program, Sterilization Processes- Physical and Chemical Processes, basic concept of microbiology, microbiological and contamination control practices


Complianceonline organises its event entitled Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers to be held from 18 June 2020 to 19 June 2020 in Dallas, TX, United States. It covers various areas of Health and Medicine including Pharmacology and Drug Development. For more information, visit the website of the conference or contact the organizer.
Add to calendar 2020-06-18 2020-06-19 Europe/London Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers https://www.sciencedz.net/en/conference/70782-cleanroom-microbiology-and-sterility-assurance-practices-for-drug-and-device-manufacturers Dallas, TX - United States Complianceonline

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Conferences and seminars in Health and Medicine in 2020
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