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Webinar On Clean Room Design and Operation

 
  February 27, 2015  
     
 


Compliance Trainings, 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
2015-03-25


Description :

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 construction 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 tags:

Live

Single Live : For One Participant

$ 249

Corporate Live : For Max. 10 Participants

$ 899

Recording

Single REC : For One Participant - Unlimited Access for 6 Months

$ 299

For more information and enquiries contact us at

Compliance Trainings

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

Like Us On Facebook:

https://www.facebook.com/events/948473101838560

 
 
Organized by: Compliance Trainings
Invited Speakers:

Speaker Profile

Tony DeMarinis has BS degrees in Biology & Microbiology and a MS in Quality Management. He is currently an independent Consultant specializing in Sterilization, Quality Systems, Auditing, and other Quality Management issues in the medical device and pharmaceutical industries. Previously, Tony was Director of QA/RA at Tunstall Americas for electronic monitoring devices, Quality Manager at Sealed Air for medical packaging, Quality Systems Manager at Davol for implants and surgical devices, Director of Quality Assurance at Scott Laboratories for in-vitro diagnostics and Sr. Microbiologist at the National Cancer Institute.

 
Deadline for Abstracts: 2015-03-25
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1363

To register this webinar

https://compliancetrainings.com/siteengine/Login.aspx

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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