Effective Internal Auditing-Making Quality Systems More Efficient forthe Medical Products Industry

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Live Webinar

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Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry

Date & Time: Thursday, October 11, 2011

10:00 AM PDT | 01:00 PM EDT

Duration: 90 Minutes

Instructor: Howard Cooper

Location: Online

Price : $245.00

Register Now

(for one participant)

Instructor Profile:

Overview: The different types of internal audits and how they are approached will be discussed. The Internal Audit Lifecycle will be followed from beginning to end. It will be shown that. Internal audits are not simple exercises to determine compliance to some regulatory standards. Instead, the focus must be on auditing the company's quality system to determine if they are meeting their objectives and are effective in resolving quality issues. Following this, value added internal auditing will be introduced. Value Added Internal Auditing VAIT) is described as going beyond the minimum requirements and also a way of actively seeking opportunities to improve the quality system. VAIT is used to improve technical processes.

Why Should You Attend: One of the primary reasons why FDA inspections are feared is that all levels of the organization feel that they do not understand or know what is going on in the facility or the fear that a very significant discovery of failure will occur.

Areas Covered in the Session: l l l l l l

Quality 101 Defining Internal Auditing. Objectives of Internal Auditing. Auditor Qualifications. Auditing Responsibilities. The Audit Lifecycle

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Value Added Auditing The Internal Audit Report

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Confidentiality of Audit Reports

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Click here to register for this webinar

David R. Dills Industry Regulatory & Compliance Consultant, Howard enjoys sharing his 30 years plus experience in starting up, developing, implementing, managing, and remediating pharmaceutical and medical device quality systems. He has a BS in Biology/Chemistry and Political Science as well as work toward an MBA. His ability to quickly learn the technology is demonstrated by his success in applying quality assurance principles to a wide range of pharmaceuticals and medical devices. He is a Certified Biomedical Auditor (CBA), Certified Quality Manager (CQM), and Quality Auditor (CQA). His technical education is further complemented by his Political Science degree helping him understand the regulatory process; his work toward an MBA provides business insight. He is a member of ASQ, PDA, AAMI, RAPS, and SQA. He strongly believes that Quality is very influential in shaping successful operations. He knows how to use his leadership abilities to build organizational relationships that make systems operate effectively as well as to develop and empower people. ...more

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Quality, quality control, regulatory, engineering, and manufacturing and IT staff working in the FDA regulated industry in the development and manufacture of medical products. Interdepartmental functions associated with scaling up and commercializing a new medical product Regulatory Affairs working on approval of combination products Suppliers and software vendors, servicing the FDA regulated industries, who want to better understand the customer’s needs and requirements.

It would be really nice if you can circulate this mail to all your deserving colleagues who can immensely benefit from this program. For more information, please contact the event coordinator. We look forward to seeing you at the webinar. Best regards, Event-coordinator GlobalCompliancePanel

About GlobalCompliancePanel


GlobalCompliancePanel is an online knowledge fulfillment community portal & it has put together a new model for online compliance training by creating a single window of learning opportunities for compliance professionals & providing a forum for expert speakers/panelists to render their services through simplified online training delivery mechanisms. Our commitment is give compliance regulatory training, showcasing of best industry practices & quality enrichment training sessions in a most cost effective manner. Compliance professionals can benefit from a wide range of training sessions, giving a diverse choice of events & all sessions being either Live or recorded stream or in the form of audio CDs. GlobalCompliancePanel portal ensures a secure & cost effective online environment and also support your E-learning and development on/through our website. Keep track of all webinars arranged for your industry through notifications & event calendars being mailed to your inbox. GlobalCompliancePanel opens new doors of learning opportunities for professionals. GlobalCompliancePanel www.globalcompliancepanel.com 1000 N West Street Suite, 1200 Wilmington DE 19801 Phone: 800-447-9407 or Fax your PO to: 302-288-6884 If you do not wish to receive this training alerts from GlobalCompliancePanel Click Unsubscribe


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