GMP Environmental Monitoring for Pharmaceutical Clean Rooms

Added by compliancetrainings on 2018-05-21

Conference Dates:

Start Date Start Date: 2018-06-11
Last Date Last Day: 2018-06-11
Deadline for abstracts/proposals Deadline for abstracts/proposals: 2018-06-08

Conference Contact Info:

Contact Person Contact Person: Alan
Email Email: [email protected]
Address Address: Online Event, Online Event, Canada
Phone Tel: 416-915-4438/ 58

Conference Description:

“In aseptic processing, one of the most important laboratory controls is the environmental monitoring program. This program provides meaningful information on the quality of the aseptic processing environment (e.g., when a given batch is being manufactured) as well as environmental trends of ancillary clean areas. Environmental monitoring should promptly identify potential routes of contamination, allowing for implementation of corrections before product contamination occurs.”

Why You Should Attend:

This webinar will first explain the various US and international regulatory requirements for various clean room classifications, as well as the environmental monitoring of clean room environments. Next, the presentation details the benefits, the regulatory requirements and the testing requirements for a comprehensive Environmental Monitoring Program.

Areas Covered in the Session :

>. Understanding Cleanroom
>. Environmental Monitoring vs. Environmental Control
>. GMP Regulations
>. Environmental Monitoring Program
-Benefits
-SOPs
-Testing Requirements
-Regulatory Classifications
-Personnel Microbial Monitoring
>. Microbiological Media Controls

Who Should Attend:

>. Quality Departments
>. Environmental Monitoring Departments
>. Microbiology
>. Manufacturing Departments
>. Validation Departments
>. Engineering Departments
>. Maintenance Departments
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