Internal and Supplier Quality System Auditing for Medical Devices

7 years ago Posted By : User Ref No: WURUR10018 0
  • Image
  • TypeSeminar
  • Image
  • Location Jersey City, New Jersey, United States
  • Price
  • Date 10-11-2016 - 11-11-2016
Internal and Supplier Quality System Auditing for Medical Devices, Jersey City, New Jersey, United States
Seminar Title
Internal and Supplier Quality System Auditing for Medical Devices
Event Type
Seminar
Seminar Date
10-11-2016 to 11-11-2016
Last Date for Applying
08-11-2016
Location
Jersey City, New Jersey, United States
Organization Name / Organize By
GlobalCompliancePanel - NetZealous LLC
Presented By
GlobalCompliancePanel
Organizing/Related Departments
NetZealous DBA as GlobalCompliancePanel
Organization Type
Training/Development
SeminarCategory
Technical
SeminarLevel
International
Related Industries

Education/Teaching/Training/Development

Biotechnology

Manufacturing

Medical/Healthcare/Hospital

OTHERS

Location
Jersey City, New Jersey, United States

OVERVIEW
Do you want to understand how to do efficient and effective internal and supplier audits that meet all the requirements of your external auditors, but also add value to your company? Are you confused by all the requirements and guidance documents for medical device quality management systems and are tired of wading through all the regulatory language they contain. This course is for those who will do internal or supplier audits, manage an audit process for these or other company audits. This course will provide you with an easy to understand presentation on the auditing process as well as the requirements you will need to audit under ISO 13485 and the FDA Quality System Regulation (cGMP)


Both FDA Quality System Regulation (QSR) and ISO 13485 require that companies do internal audits. However, because the FDA does not look at the content of internal audits, some companies do not get feedback on the true effectiveness of their internal audit system from the FDA during FDA Inspections. ISO 13485 auditors do look at internal audits, but are most concerned that you define a process that meets the requirements of the standard and are following your process. Both require that you define Auditor training is required, but this sometimes just requires reading the company's procedure, although most external auditors will look for more than this.


Do you need to train new auditors for yours medical device quality management system or to audit your suppliers? Or do you need to improve the training of your internal and supplier auditors so that they add value to these audits? If you need to do either of these, this seminar will provide this training. In addition to auditing skills and hands-on auditing exercises, this seminar will provide an overview of the requirements for Quality Management Systems (QMS) for both the FDA and ISO 13485, because auditors need to understand the requirements for the audits they conduct. This seminar will also cover the best practices for creating and managing a value-added auditing process that will meet both company business needs and regulatory requirements


In this seminar you will review all the quality management system requirements of FDA and ISO 13485 and then learn how to set up and manage an audit system that complies with these requirements, yet is risk-based so that your company makes the most efficient use of auditing resources for both internal and supplier audits. The seminar will include interactive exercises to reinforce the fundamentals of conducting and documenting quality system audits. Auditing principles taught in this seminar will be based on ISO 19011:2011 Guidelines for auditing management systems.

WHY SHOULD YOU ATTEND:
Internal and supplier audits are effective and efficient ways for your company to stay in compliance with ISO 13485 and or FDA Quality System Regulation requirements. They help you spot problems or potential problems before they become large issues and before they are found by external auditors. Therefore, it is of great benefit to companies to make sure their internal and supplier audits are trained in applicable standards, regulations, and the auditing process. It is also important that you establish and maintain an audit program that covers all requirements, both external and internal. Effective internal and supplier audits make good business sense.


This course is designed for people who preform or manage audits of a medical device quality management system, including internal and or supplier audits. Both 21 CFR 820 Quality Systems Regulation (cGMP) and ISO13485 and Quality Management Systems auditing will be covered.
This course will be particularly helpful to the following

  • Senior quality managers who need to establish or manage an audit program
  • Quality professionals who need to know how to conduct effective internal or supplier audits
  • Regulatory professionals responsible for compliance
  • Internal or supplier auditors who need a better understanding of the auditing processor medical device quality management system requirements
  • New internal or supplier auditors
  • Audit Managers who need to update or streamline your internal auditing process
  • All Managers who need to establish an internal or supplier audit program

AREAS COVERED IN THE SESSION:

  • Understand the basic requirements of FDA cGMP/ Quality System Regulation and ISO 13485 which are the basis for what must be audited in your internal audit program
  • Be able to develop or update and internal auditing system that is compliant to FDA cGMP/ Quality System Regulation and ISO 13485, yet makes efficient use of company resources
  • Understand how to manage an Internal Audit system
  • Understand the difference between internal and external audits
  • Learn how the internal auditing system can add value to your quality system and your company
  • Learn how using a risk-based process can make your audits more efficient and effective
  • Learn how an effective audit system can be an integral part of continuously improving your quality system and your company
  • Understand what makes a good internal audit
  • Understand and have a chance to practice the skills required for an internal or supplier auditor
  • Understand and have a chance to practice how to write effective audit non-conformances
  • Understand what the FDA must see to verify that you are conducting your internal audits as required

WHO WILL BENEFIT:

  • Quality Managers
  • Quality Engineers
  • Audit Managers
  • Supplier Engineers
  • Internal quality auditors
  • Supplier auditors
  • Quality associates
  • Quality Specialists
  • Regulatory Compliance Managers

Others Details

For Seminar schedule, more details and updates please visit website

Registration Fees
Available
Registration Fees Details
Price: $1,295.00 (Seminar for One Delegate) Until September 15, Early Bird Price: $1,295.00 from September 16 to November 8, Regular Price: $1,495.00 Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*
Registration Ways
Email
Phone
Website
Address/Venue
  Courtyard Jersey City Newport 540 Washington Boulevard. Jersey City, New Jersey, United States  Pin/Zip Code : NJ 07310
Official Email ID
Contact
John Robinson

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

[email protected]

     +1-800-447-9407
   Fax No: 302-288-6884
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