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Design Control for Medical Device Professionals

 
  January 19, 2018  
     
 
CfPIE - The Center for Professional Innovation & Education, Berlin, Germany
29 & 30 May, 2018


Course Description - Course runs 9:00 to 5:00 both days (Breakfast & Lunch Included)

This continually updated course covers design control for medical devices in accordance with current FDA regulations. A focus will be placed on basic regulation and the FDA's supplemental guidelines.

Among the topics to be discussed are: context of design control within the overall quality system and regulation, design control procedures, forms, records, safety/risk management strategies, documentation strategies, manufacturing transfer strategies, and strategies for integrating general quality system procedures into design control.

Who Should Attend

This course will be most valuable to medical device industry engineers, engineering managers, regulatory affairs professionals, scientists, and quality engineers needing an understanding of Design Control per the FDA's CFR 820.30. The course also provides context for 820.30 vs. the Design Control part of ISO 13485:2003.

Personnel involved in product development, manufacturing, quality assurance, or regulatory affairs that do not have an in-depth knowledge of the design control for medical devices, as well as its workings, will benefit from this course. Additionally, this program can be customized and delivered on-site for more experienced personnel (including middle and upper management) to update and broaden their knowledge of the FDA's Design Control requirements.

 
 
Organized by: Center for Professional Innovation & Education
Invited Speakers:

Jim Rosa

Specialties: Medical Devices, Regulatory

Jim Rosa provides quality engineering guidance to companies for the development, management and operation of quality systems for devices.  He has 40 years of experience leading R&D and quality functions within regulated industries.  With roots in research and development and conversion to quality systems oversight later in his career, Jim provides a solid understanding and perspective from engineering and quality in bringing products to market in the medical device and IVD industries.  The blend of working with research & development and quality system function, in the EU and US, in startups and large companies provides a unique insight into the practical application of design control for medical devices.  Jim also has four patents related to medical device safety system implementations.  Jim has worked for Gambro, Intel, Reglera, Dohmen and a number of start-ups such as CeMines (IVD) and FibroTx(IVD).

Jim’s recent focus has been on Systems & Software within the medical device market, driving strategy and implementation efforts for traditional electromechanical, mobile applications, wireless applications, infrastructure software devices, and software as a device.  Additionally, Jim has taught Design Controls, V&V, and Risk Management at the University level.

Mr. Rosa has earned degrees from Colorado State University (MBA) and the Radford University (BSCS).

 
Deadline for Abstracts: N/A
 
Registration: https://www.cfpie.com/ProductDetails.aspx?ProductID=226
E-mail: info@cfpie.com
 
 
   
 
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