Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
2020 - Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
Date2020-06-18 - 2020-06-19
Deadline2020-06-08
VenueDallas, TX, USA - United States 
KeywordsCleanroom regulations; Cleanroom classifications; Cleanroom qualification
Topics/Call fo Papers
Discuss Cleanroom Classification, Regulations and Guidelines
Summarize how to Perform Cleanroom Design, Validation/Qualification, Operation, Environmental Monitoring Program and ensuring a state of control
Describe Aseptic Practices, Personnel Health Practices, Gowning and Trafficking Patterns in a Cleanroom
Establish and describe the Requirements of Cleanroom Cleaning/Disinfection and Contamination Control Practices
Summarize various Sterilization Processes, Advantages and Disadvantages –both Physical and Chemical
Describe the Sterilization Processes and Controls
Summarize how to Perform Cleanroom Design, Validation/Qualification, Operation, Environmental Monitoring Program and ensuring a state of control
Describe Aseptic Practices, Personnel Health Practices, Gowning and Trafficking Patterns in a Cleanroom
Establish and describe the Requirements of Cleanroom Cleaning/Disinfection and Contamination Control Practices
Summarize various Sterilization Processes, Advantages and Disadvantages –both Physical and Chemical
Describe the Sterilization Processes and Controls
Other CFPs
- Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
- How to Conduct an ACH Risk Assessment and Develop an Effective ACH Risk Management Program
- Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
- 21 CFR Part 11 Compliance for SaaS/Cloud Applications
- REACH and RoHS Compliance: Gain a Deeper Understanding
Last modified: 2020-05-02 22:50:14