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2-day In-person Seminar on “Quality Audits for the Medical Device Industry” at Raleigh, NC

 
  September 01, 2014  
     
 


GlobalCompliancePanel, 1041 Wake Towne Dr, Raleigh, NC 27609, United States
2014-10-30


Summary of the workshop:

Quality audits are an important element in checking the health of a Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure on effective QMS.

When you read an FDA Warning Letter do you ask, "Where was the internal audit program?" Why didn't the company find it themselves?

In this seminar participants will look at the various kinds of audits and understand their role. Internal quality audits (1st party) help a company evaluate itself. Customer/supplier audits (2nd party) play a role in an effective supplier management program. Don't forget that you could be the supplier being audited. Independent audits (3rd party) can help provide assurance about the health of a QMS.

 

Learning Objectives:

This seminar will help you create an effective quality audit program for medical device manufacturing. Your audit program needs two major elements. First, you need a plan to schedule, conduct, report, and close audits. Second, you need qualified people to perform the audits. The seminar explains how to implement the quality audit program elements using examples and exercises that help develop the necessary skills.

Another important part of an audit program is responding to audit non-conformances. This includes correction, investigation, and corrective action. An effective audit program will determine and eliminate the cause of the nonconformity. These methods are important in all three audits types. The seminar provides methods and exercises to help implement these important activities.

Management needs to understand the results from each audit type, which are presented at Management Review. The presentation should use statistical methodology to analyse quality audit reports. The seminar discusses the role of management review and helps you identify the appropriate statistical methodology.

RAC Credits: 12

Date: October 30th & 31st, 2014 

Event Details: http://bit.ly/QualityAuditsfortheMedicalDeviceIndustry  

Location: Raleigh, NC

Venue: Courtyard Raleigh Midtown

Venue Address:  1041 Wake Towne Dr, Raleigh, NC 27609, United States

Registration: Open Enrollment

Delivery: Face-to-Face event

Price: $1295.00

Until September 15, Early Bird Price: $1,295.00

From September 16 to October 28, Regular Price: $1,495.00

 

Audience: Senior and middle management, Management Representative, Quality Assurance, Quality Engineers, Regulatory Affairs, Supplier Management and Purchasing, Supplier Quality Engineers, Lead Auditors, Audit Team Members.

 

Course Web Site: https://www.globalcompliancepanel.com/control/~product_id=900107SEMINAR/quality-audits-medical-device-industry

Organizer:
GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management.

Our Achievements:

Over 300 Experts that are Renowned in their Respective Areas

Successfully Trained more than 20,000 Compliance Professionals

A Most Comprehensive Portal for Trainings, Industry Updates and Professional Growth

Having more than 2000 Online Courses

Successfully Completed more than 170 Seminars in US and Globally

 

Provider:

GlobalCompliancePanel

                John Robinson

                161 Mission Falls Lane, Suite 216, Fremont, CA 94539, USA

                Phone: 1800-447-9407

                Fax: 302-288-6884

                Email: support@globalcompliancepanel.com

                Website: www.globalcompliancepanel.com

  

 
 
Organized by: GlobalCompliancePanel
Invited Speakers:

Meet your Expert:

Dan O'Leary is the President of Ombu Enterprises, LLC, a company offering training and execution in Operational Excellence, focused on analytic skills and a systems approach to operations management. Dan has more than 30 year’s experience in quality, operations, and program management in regulated industries including aviation, defence, medical devices, and clinical labs. He has a Master’s Degree in Mathematics; is an ASQ certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer, and Six Sigma Black Belt; and is certified by APICS in Resource Management.

 

 
Deadline for Abstracts: 2014-10-30
 
Registration:

Date: October 30th & 31st, 2014 

Event Details: http://bit.ly/QualityAuditsfortheMedicalDeviceIndustry  

Phone: 1800-447-9407

                Fax: 302-288-6884

                Email: support@globalcompliancepanel.com

                Website: www.globalcompliancepanel.com 

E-mail: support@globalcompliancepanel.com
 
   
 
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