This continually updated course covers current FDA regulatory compliance with respect to developing medical devices. 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.
This course has been pre-approved by the Regulatory Affairs Professionals Society (RAPS) as eligible for 12 credits towards a participant's RAC recertification upon full completion.
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, and 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.
Introduction to Design Control
Quality System Aspects
Integrated Risk Management
Implementing Top Level Design Control Procedure
Validation and Verification (V&V)
Integrating General Quality Procedures in Design Control
Upon completion of this course, attendees will have an understanding of the framework for Design Control and recommendations to effectively meet the requirements of Design Control. Emphasis will be placed not only on regulatory aspects but on effective design strategy, which is very important to avoid spending unnecessary time and money on an ineffective design control process.
Through the use of interactive instruction, this course will cover the general context for design control, quality systems, standards, and recommended design control procedures. Special attention is given to implementation aspects of key parts of design control. Manufacturing transfer and general quality system topics will be covered as they relate to the design process. Several exercises will be completed by attendees to reinforce key concepts. Participants will receive extensive course notes that are designed to be used as reference material once the course is completed.
"Course addressed a variety of useful and interesting topics. Covered all aspects of design control. Interesting and challenging exercises." Andrew R., Scientific & Regulatory Affairs Manager, MLT Research Ltd
"This course was extremely thorough. Design controls are now completely understood. The course was extremely informative. The instructor knew the topic and passed on his knowledge. All things were presented in a professional and excellent manner. The Course Director is a wonderful teacher." Christine W., Design Drafter, EBI, LP
"This course was extremely thorough. Design controls are now completely understood. The course was extremely informative. The instructor knew the topic and passed on his knowledge. All things were presented in a professional and excellent manner. The Course Director is a wonderful teacher." Christine W., Design Drafter, Biomet
"The Course Director was very knowledgeable of the design control process. He answered all my questions thoroughly." Angela W. , Sr. Product Development Engineer, Surgical Specialties
"Excellent course. Small number of students was very helpful in engaging in discussion, etc." Andrew B., Senior Regional Auditor, Pfizer U.K.
"I came into the course wondering how I could link design control concepts to QC testing of reagents in a diagnostic test that is being developed in my company. I feel that the course material and the way in which it was taught definitely helped me understand how I can get my job done more efficiently and what is really required in order to adequately assess various risk management issues as they relate to the above mentioned diagnostic test." Thomas V., Product Development Scientist III
"Excellent course. Small number of students was very helpful in engaging in discussion, etc." Andrew B., Senior Regional Auditor, Pfizer U. K.
"This course was a real eye-opener for many of our Design Team. The exercise with statistics for validation was fantastic and will really help us with validation. Thank you!" Patricia H., Quality Technician, Tecan Systems
"The course was very concise and the instructor was very knowledgeable. I would recommend this highly. There was a good general understanding for FDA manufacturing requirements." Greg V., Quality Assurance Engineer, Roche
"The templates were tremendously helpful. The Course Director's suggestions on methods to develop clear design inputs, and the emphasis on the importance of clear design inputs, were very useful." Julie W., Validation Team, Biomimetic Therapeutics
Yes. The Design Validation, Verification, and Risk Analysis course provides a deeper, narrower, and more strategic look at the topics of Validation, Verification, and Risk Analysis as compared to the Design Control course. The Design Control course covers greater breadth and a more comprehensive overall view of Design Controls. The two courses are intended to be complimentary.
The course does discuss the relationship between the ISO 13485-2003 and FDA's 21 cfr part 820 regulation. After a comparison is established, the course materials follow FDA's 21 cfr part 820.30 references partly because the regulation and the corresponding guidance documents are publicly available without purchase.
A course notebook is provided that contains the slides that are presented, publicly available reference materials from FDA and other entities, class exercises, and example documents and procedures.
No. A wide variety of medical device types are affected by the regulation, thus a broad view is presented.
A short but broad overview of key medical device regulations that relate in some way to Design Controls are presented in order to provide additional context for the course.
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*Valid up to 30 days prior to course date(s). Cannot be combined with other discounts or offers.
The Center for Professional Innovation and Education (CfPIE) provides technical training for Pharmaceutical, Biotech, Medical Device and Skin/Cosmetics professionals. CfPIE offers more than 350 class sessions annually across 80 course titles in multiple formats, such as classroom, on-site and certification programs.
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