Aspects to Consider for Clean Room Qualification and Operation

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Aspects to Consider for Clean Room Qualification and Operation - Webinar By GlobalCompliancePanel

Website webinars@globalcompliancepanel.com | Edit Freely

Category online training,Clean Room Qualification and Operation,Interlocks and Pass Throughs,clinical,QA

Deadline: May 15, 2012 | Date: May 15, 2012

Venue/Country: Online Training, U.S.A

Updated: 2012-04-09 20:09:16 (GMT+9)

Call For Papers - CFP

Overview: Controlled environmental conditions are often used when making medical devices and pharmaceuticals. However, to make sure these clean rooms are continuously operating in a state of control can be a difficult task unless the appropriate controls are incorporated into the design.

This talk will focus on the controls that need to be considered during the design and contruction and the methods to demonstrate these controls are effective.

Areas Covered in the Session:

Clean Room Classification Design and Operation

Engineering and Budget Considerations

Air Filtration and Maintaining Positive Pressure

Interlocks and Pass Throughs

Controlling Human Factors

Acceptance Criteria

Who Will Benefit: This discussion will benefit any organization that wants to improve the control of their current clean room faclity or those considering building or upgradeing their clean rooms. It should be of interest to:

QA and Manufacturing Managers

Engineers

Supervisors

consultants

Auditors responsible for designing or qualifying controlled environments or operating within them

Price List:

Live : $245.00

Corporate live : $995.00

Recorded : $295.00

webinarsglobalcompliancepanel.com

http://www.globalcompliancepanel.com

Phone: 800-447-9407

Fax: 302-288-6884

1000 N West Street | Suite 1200 | Wilmington | DE | USA | 19801

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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