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COVID CANCELLED: Project Management in Human Resources, Boston MA, Jan 6-8, 2021
COVID CANCELLED: InterDrone, The International Drone Conference, Cambridge MA, Jan 11-13, 2021
COVID CANCELLED: Supplier Management for Medical Device Manufacturers, Cambridge MA, Feb 2-4, 2021
COVID CANCELLED: US Immigration Compliance Strategies, Boston MA, Feb 15-18, 2021
COVID CANCELLED: Project Management Training, Boston MA, Mar 3-5, 2021
COVID CANCELLED: Internal Audit, Fraud Risk Assessment Workshop, Boston MA, Mar 22-25, 2021
COVID CANCELLED: Agile / Scrum Training, Boston MA, Apr 12-14, 2021
COVID CANCELLED: Validation, Verification and Transfer of Analytical Methods, Boston MA, Apr 19-21, 2021
COVID CANCELLED: Computer System Validation - Reduce Costs and Avoid 483s, Boston MA, May 10-12, 2021
COVID CANCELLED: SharePoint Technology Conference, Boston MA, May 26-28, 2021
COVID CANCELLED: Employment Laws Certificate Program, Boston MA, Jun 7-9, 2021
Following events are tentatively planned but may be rescheduled, based on CDC guidelines or attendee registration interest .
TENTATIVE: 21 CFR Part 11 Compliance, Boston MA, Sep 22-24, 2021
TENTATIVE: Quality Control Laboratory Compliance, Boston MA, Oct 6-8, 2021
TENTATIVE: Analytical Instrument Qualification and System Validation, Boston MA, Nov 15-17, 2021
TENTATIVE: FDA's New Import Program for 2021, Boston MA, Dec 7-9, 2021
Boston Professional Events List
Live Webinar 60 minutes Environmental Monitoring Investigations
Link to Website
This webinar will provide an overview of environmental monitoring investigations and tools to complete an investigation. Environmental monitoring is the method by which clean rooms are known to maintain a certain level of cleanliness. The methods by which clean rooms are monitored are through viable and non-viable testing. Through this testing, a room may demonstrate that it is out of control. This seminar will provide aspects to investigate and determine a root cause, as well as, appropriate actions to complete the report.
Why should you attend
Understanding how your clean room operates is the key to getting through an inspection. An inspector with expect you to conduct a comprehensive report and put the proper actions into place. This webinar will provide the tools necessary to have that comprehensive report the inspector is looking for and provide appropriate corrective actions for the various excursion types.
International regulations (ISO)
Federal regulation (FDA, USP)
Identification of microorganisms
Determination of a root cause
Corrective and Preventative actions to put into place
Provide background information on regulatory guidance on environmental monitoring.
Provide background information on environmental monitoring methods for viable and non-viable testing.
Correlate non-viable and viable results with the appropriate environmental monitoring controls.
Provide possible sources of contamination and possible corrective actions.
Provide possible preventative actions in order to prevent future contamination
Provide case studies on contamination events.
Who will benefit
Pharmaceutical Manufacturing Companies
Contract Manufacturing Companies (CMOs)
Personnel Involved with Environmental Monitoring Operations
Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance Professional who is based in San Diego, California.
(Contact us : 844-267-7299 | 954-947-5671
Don't wait. Register TODAY or Email US [email protected]
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