Online Webinar on ISO5 2014 - ISO 13485: 2003 - A Straightforward Interpretation with Recommendations for Easy Implementation
Date2014-07-15
Deadline2014-07-15
VenueOnline Event, USA - United States
KeywordsCompliance Training; Regulatory Training; Pharma; Clinical; Health
Websitehttps://bit.ly/1nnq2cA
Topics/Call fo Papers
Overview:
Development, implementation, and maintenance of an ISO 13485-compliant quality management system requires many resources and personnel to meet with success.
ISO 13485 is a wordy standard, drafted by individuals for many of whom English is not their primary language. This webinar is a section-by-section review of ISO 13485 in a clear concise manner, and provides suggestions for development of a compliant system.
Areas Covered in the Session:
The purpose of the standard
The structure of the standard
The requirements of the standard
Straightforward recommended implementation approach
Who Will Benefit:
This webinar will provide valuable assistance to all device manufacturers who wish to have a better understanding of the requirements of ISO 13485. The employees who will benefit include:
Top management
Regulatory Management
Quality Management
Documentation Managers
Quality Engineers
Other personnel involved in development and implementation of the QMS
Quick Contact:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Link - bit.ly/1nnq2cA
Development, implementation, and maintenance of an ISO 13485-compliant quality management system requires many resources and personnel to meet with success.
ISO 13485 is a wordy standard, drafted by individuals for many of whom English is not their primary language. This webinar is a section-by-section review of ISO 13485 in a clear concise manner, and provides suggestions for development of a compliant system.
Areas Covered in the Session:
The purpose of the standard
The structure of the standard
The requirements of the standard
Straightforward recommended implementation approach
Who Will Benefit:
This webinar will provide valuable assistance to all device manufacturers who wish to have a better understanding of the requirements of ISO 13485. The employees who will benefit include:
Top management
Regulatory Management
Quality Management
Documentation Managers
Quality Engineers
Other personnel involved in development and implementation of the QMS
Quick Contact:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Link - bit.ly/1nnq2cA
Other CFPs
- Managing the IDE (Investigational Device Exemption) Submission for Compliance Success
- HACCP Validation and Verification
- Understanding and Preparing for FDA's on-going Part 11 Inspection Program
- Meet FDA Expectations for a Tougher Supplier Audit Program
- 2014 International Conference on Education and Modern Educational Technologies
Last modified: 2014-06-06 13:52:45