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Live Webinar Risk Based Environmental Monitoring

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Website https://worldcomplianceseminars.com/webinardetails/173 | Edit Freely

Category

Deadline: May 29, 2018 | Date: May 29, 2018

Venue/Country: Online, U.S.A

Updated: 2018-05-08 16:44:38 (GMT+9)

Call For Papers - CFP

Live Webinar Risk Based Environmental Monitoring

Time: 01:00 PM EDT | 10:00 AM PDT | 12:00 PM CDT Duration 90 Minutes

Description

Environmental Monitoring (EM) programs for pharmaceutical manufacturing are evolving to a risk-based approach. The use of sampling data for the identification and mitigation of risk becomes a critical element in this process. No longer is it enough to utilize data for reactive excursion reporting.

Areas Covered

This presentation will discuss how to establish a risk-based Environmental Monitoring Program. During this session we will discuss how to set up a new Environmental Monitoring Program based on risk as well as how to perform a reassessment of your current Environmental Monitoring Program to re-establish sampling locations and frequencies based on results of your risk assessments coupled with the knowledge gained from your current EM Program historical data.

Key Learning Objectives of your Topic:

• Current regulatory requirements for environmental monitoring

• How to select sample locations based on risk

• How to perform a risk assessment to support your EM Program

• Differences in room classifications and impact to your EM Program

• Monitoring methods, equipment and media types

• Data collection, microbial identifications and data trending options

Who will Benefit

• Environmental Monitoring Samplers/Managers

• Quality Assurance/Quality Control professionals

• Sterility Assurance professionals

Speaker Profile

Danielle DeLucy, MS, is currently an independent consultant to the biologics and pharmaceutical industries specializing in the areas of quality assurance and quality systems. Prior to this role, Ms. DeLucy has been in the industry for 15 years serving in numerous quality management roles, such as the director of product quality, the oversight of sterility assurance practices and provided QA oversight of numerous filling and packaging operations.

Price: $179 One Dial-in One Attendee | Corporate Live Recorded $279 One Dial In - Max 10 attendees |Group $695 Multiple locations upto 5 dial in | Recorded $249


Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.