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ISO 14971 Co-Author to Conduct ComplianceOnline Seminar on Medical Device Risk Management

ComplianceOnline, the leading GRC advisory network and former FDA Medical Device Laboratories Deputy Director and co-author of ISO 14971:2000 Dr. Harvey Rudolph will conduct a one and half day seminar on Medical Device Risk Management.

 
PRLog - Nov. 28, 2012 - Palo Alto, CA, USA – November 28, 2012 -ComplianceOnline, the leading compliance training provider for life science companies , today announced a seminar Medical Device (http://www.complianceonline.com/ecommerce/control/seminar?product_id=80076SEM&channel=PR_Nov%2028) Risk Management A to Z - Best Practices for Effectiveness and Efficiency. The one and half a day seminar by former FDA Medical Device Laboratory Deputy Director Harvey Rudolph will be held on January 24 and 25, 2013 in San Francisco, CA.For more information or to register for the seminar, please click here (http://www.complianceonline.com/ecommerce/control/seminar...).

Seminar instructor Dr. Harvey Rudolph is an independent risk management consultant specializing in process development and training in risk management. He worked at the FDA for 25 years where he retired as deputy director of the medical device laboratories. He has been a member of the Joint Working Group on Risk Management since it began in 1995 and is a primary author of ISO 14971. Currently he co-chairs the US Technical Advisory Group for that standard and is working on the new ISO risk management guidance document.

During the one and half a day seminar Dr Rudolph will focus on the reasons for risk management and the central role it plays in the product life cycle. The interactive workshop would take the attendees through all of the risk management activities required by ISO 14971. He will also discuss on the requirements of ISO 14971 and the ways to meet them. He will also give practical exercises on efficient and effective use of risk management.

The seminar will be valuable for project managers, quality managers, R & D managers, regulatory and compliance managers and anyone with risk management responsibilities.

Date: Thursday, January 24 (8.30 AM- 5PM PST) and Friday, January 25, 2013 (8.30 AM- 1PM PST)

Venue & Location: Grand Hyatt, San Francisco, CA

Registration Cost: $1,199per registration

Early bird discounts: For discounts on early registrations, please click here.

Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to customercare@complianceonline.com

For more information on ComplianceOnline or to browse through our trainings, please visit our website (http://www.complianceonline.com/?channel=PR_Nov28)

About ComplianceOnline
ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 20,000 professionals from 3,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at http://www.complianceonline.com.

For more information please contact:

A Reuben Bernard

Manager of Program Marketing

ComplianceOnline

2600 E Bayshore Rd

Palo Alto CA USA 94303

650-620-3937 phone

650-963-2530 fax

reuben@complianceonline.com  

http://www.complianceonline.com

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Contact Email:
***@complianceonline.com Email Verified
Source:ComplianceOnline
Phone:+1-650-620-3915
Zip:94303
City/Town:Palo Alto - California - United States
Industry:Medical
Tags:ISO 14971, medical device
Shortcut:prlog.org/12032165
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