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

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. 

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. 

RAC Credits: 12

Date: October 30^th & 31^st, 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

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. 

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