AN FDA INSPECTION WILL FOCUS ON THE RECORDS YOU MA 2013 - Live Web Seminar on Understanding Device Master Records and Device History Records for Medical Devices By Dan O’Leary

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Category Biotechnology

Deadline: April 09, 2013 | Date: April 10, 2013

Venue/Country: Houston, U.S.A

Updated: 2013-02-15 17:32:52 (GMT+9)

Call For Papers - CFP

An FDA inspection will focus on the records you maintain. These records provide the objective evidence that demonstrates your QMS operates the way it should. While procedures are important, the supporting records demonstrate that you follow your own procedures.

Much of the evidence is in the four records we discuss in the webinar. If you determine what you keep in each record and then follow your decision, you will have the evidence that you need. Moreover, a well organized set of records will help you lower cost in the QMS and provide valuable information when you need to investigate a problem and take corrective action.

Your Quality Management System (QMS) should be able to address these questions quickly and easily. If not, then your team needs to attend this webinar!

? Can you list the kinds of records that belong in the Design History File (DHF)?

? Can your team relate the component specifications in the DMR to the Purchasing Data you use to obtain the components?

? Does your team know the records you must keep when you verify the component at receiving?

? Does you team know which of these records must go into the DHR?

? Can your team list the activities that require a designated individual?

? Do you have quality records that designate the individual and demonstrate training to perform the assigned responsibility?

? Can you list the activities and the designated individuals in your company?

? Can your team assure that the designated individual, not somebody else, performed the activity before you released the product for distribution?

? Some information could be in the DMR or the QSR. Does you team know how to make the decision?

Description of the topic

The FDA’s Quality System Regulation (QSR) requires each device manufacturer to compile the specifications and procedures for a medical device. The manufacturer must also compile records of the production history of the device. These two sets of records (DMR & DHR) are complimentary. In addition, the manufacturer maintains two more sets of documents, the Design History File (DHF) and the Quality System Record (QSR). This webinar explains these requirements from QSR and explains the role of each document type. The webinar uses the QSR preamble to explore FDA’s thinking, FDA guidance documents for recommendations, and Warning Letters to help participants learn from other firm’s experience.

Areas Covered in the Session

? The FDA’s QSR

o The source of the requirements

o The preamble

o The QSR Manual

o OMB information collection

? Key Definitions

? Design History File (DHF)

o Requirements

o Content

? Quality System Record (QSR)

? Device Master Record (DMR)

o Contents

o Linkage to Design Controls

o Lessons for Implementation

? Device History Record (DHR)

o Contents

o Linkage to the DMR

o Lessons for Implementation

Webinar Includes:

- Q/A Session with the expert

- PDF copy for the presentation materials

- 90 Minutes Live Webinar

Who will benefit (Titles)

This seminar is for people involved in project management, design, production, purchasing, installation, servicing, document control, and record keeping activities for medical device manufacturing.

People in the following roles can especially benefit from the knowledge in this webinar:

? Quality Managers

? Quality Professionals

? Regulatory Professionals

? Production Managers

? Risk Managers

? Project Managers

? Production Supervisors

? Manufacturing Engineers

? Production Engineers

? Design Engineers

? Process Owners

? Quality Engineers

? Quality Auditors

? Document Control Specialists

Record Retention Specialists

About Speaker

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 years experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs. He has a Masters Degree in Mathematics; is an ASQ certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer, and Six Sigma Black Belt; and holds an APICS certification in Resource Management.

Speaker : Dan O’Leary

Product ID : M62047

Schedule Date :

Wednesday, April 10, 2013

duration : 01:00 to 02:30 PM EDT

https://compliance2go.com/index.php?option=com_training&speakerkey=25&productKey=92