Webinar on Supplier Management 2014 - Best Practices in Supplier Management
Date2014-07-29
Deadline2014-07-29
VenueOnline Event, USA - United States
KeywordsCompliance Training; Regulatory Training; Pharma; Clinical; Health
Websitehttps://bit.ly/1lMoAvY
Topics/Call fo Papers
Overview:
Supplier qualification and assessment is required in both the QSR regulations and ISO standards.
Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.
Areas Covered in the Session:
QSR and ISO 13485 requirements for supplier selection and assessment
How to qualify new suppliers in a cost efficient manner
How to assess current suppliers in a cost efficient manner
How to perform supplier-related corrective action
Minimum documentation requirements for supplier qualification, assessment, and related corrective action
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. The employees who will benefit include:
Purchasing management
Regulatory management
QA management
Consultants
Quick Contact:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Link - http://bit.ly/1lMoAvY
Supplier qualification and assessment is required in both the QSR regulations and ISO standards.
Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier evaluation and assessment, and provide cost efficient, equally compliant options to many of the most common practices.
Areas Covered in the Session:
QSR and ISO 13485 requirements for supplier selection and assessment
How to qualify new suppliers in a cost efficient manner
How to assess current suppliers in a cost efficient manner
How to perform supplier-related corrective action
Minimum documentation requirements for supplier qualification, assessment, and related corrective action
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that are interested in incurring less cost on supplier evaluation and assessment. The employees who will benefit include:
Purchasing management
Regulatory management
QA management
Consultants
Quick Contact:
GlobalCompliancePanel
USA Phone:800-447-9407
Fax: 302-288-6884
webinars-AT-globalcompliancepanel.com
http://www.globalcompliancepanel.com
Event Link - http://bit.ly/1lMoAvY
Other CFPs
- How to Conduct a Hazard Analysis/Risk Assessment
- Update on FDA 510(k) Review Process, Hurdles and Good Practices on 510(k) Preparation and Clearance
- ISO 13485: 2003 - A Straightforward Interpretation with Recommendations for Easy Implementation
- Managing the IDE (Investigational Device Exemption) Submission for Compliance Success
- HACCP Validation and Verification
Last modified: 2014-06-06 14:00:08