Human Factors Methods and Device Product Life Cycle 2017
Event on 2017-07-20 09:00:00
Course "Human Factors and Predicate Combination Products" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
The FDA has placed significant emphasis on the role of Human Factors in the approval of devices used for medical purposes. There are several current guidance documents and new proposed Draft Guidance documents. This seminar will compare these Guidance documents. Additionally, strategic recommendations will be presented on how to implement these requirements into the medical device design, development and approval processes. Finally, Human Factors methods and best practices will be covered that the FDA is requiring.
Why should you attend :
Are you familiar with the role of Human Factors with respect to combination products and the FDA requirements? Are you current on the FDA's current perspectives on Human Factors? Human Factors has become increasingly important to the FDAs approval of medical devices. It is a part of the design and development of the device and the collateral information, e.g., labeling, IFUs, and training. Incorporating Human Factors into the device development process can get a product to market faster and cost less. Hence, this seminar will cover all of the current and future Human Factors FDA requirements and show how to not increase costs or time.
Areas Covered in the Session:
• Overview of Human Factors and the FDA perspective
• Human Factors Methods and Device Product Life Cycle
• Human Factors and Risk Analysis & Management
• Human Factors: What Devices Require Human Factors Evaluation and Validation?
• Human Factors and Combination Products
• Human Factors and Combination Products Submitted in an ANDA
Who will benefit:
• Qualtiy Assurance
• Regulatory Affairs
• Device Engineers
• Device Manufacturers
• Pharma / Medical Device
Day 1 Schedule
Overview of Human Factors and the FDA perspective
Human Factors Methods and Device Product Life Cycle
Human Factors and Risk Analysis & Management
Human Factors: What Devices Require Human Factors Evaluation and Validation?
Day 2 Schedule
Human Factors and Combination Products (Part 1)
Human Factors and Combination Products (Part 2)
Human Factors and Combination Products Submitted in an ANDA (Part 1)
Human Factors and Combination Products Submitted in an ANDA (Part 2)
Virginia A. Lang
Principal and Founder HirLan, Inc. and HirLan International SA
Virginia started in the medical research field as a Coordinator of Research at the Clinical Research Unit Kennedy Institute of Johns Hopkins Medical Center. She was responsible for the initiation, coordination, and management and/or analysis of research projects in the Clinical Research Unit. These projects were funded by various Federal Government Agencies. Subsequent to Johns Hopkins Medical Center, Virginia entered the field of Human Factors through the doctoral program at SUNY Binghamton. Virginia held a fellowship at the Aeromedical Research Laboratory of the United States Air Force at Wright-Patterson AFB, Dayton, Ohio and a fellowship at NASA. Her research dealt with cognitive factors that differentially affect the characteristics of visual displays. Applications of this research are directly related to various medical devices and software applications providing Medical Device Human Factors by HirLan clients with 30 years of Human Factors experience.
In addition, Virginia has extensive experience in the areas of product design, Customer Centered Participatory Design processes, and product lifecycle management. She is also known in the Human Computer Interaction and Usability Communities for her innovative techniques for collecting and incorporating user/customer feedback throughout the product lifecycle. In July 2014, Virginia founded and established the HirLan Institute of Human Factors with labs in Carlsbad, California and a Consortium arrangement in London, UK. In February 2013, Virginia founded HirLan International SA, a Geneva, Switzerland based company. Both HirLan and HirLan International have been supporting Top Ten pharma/medical device companies, as well as, start-ups with consulting and testing services. These services are in conjunction with their clients? FDA 510(k) and CE mark applications.
Virginia holds a PhD in Cognitive-Experimental Psychology from SUNY Binghamton, and a Master of Science (ABT) in Applied Technology, Systems Science from SUNY Binghamton.
Location: Washington DC Date: July 20th & 21st, 2017 and Time: 9:00 AM to 6:00 PM
Venue: Courtyard Arlington Crystal City/Reagan National Airport
Address: 2899 Jefferson Davis Highway Arlington, VA 22202 USA
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Price: ,295.00 (Seminar Fee for One Delegate)
Until June 10, Early Bird Price: ,295.00 From June 11 to July 18, Regular Price: ,495.00
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Sponsorship Program benefits for “Human Factors and Predicate Combination Products” seminar
At this seminar, world-renowned Human Factors and Predicate Combination Products subject matter experts interact with CXO’s of various designations. Executives who carry vast experience about Human Factors and Experts get down to discussing industry-related best practices, regulatory updates, changes in technologies, and much more relating to Human Factors.
As a sponsor of these seminars, you get the opportunity to have your product and company reach out to C-Level executives in Human Factors industries and become known among these elite executives and subject matter experts. Apart from being seen prominently at these globally held seminars, you also get talked about frequently in our correspondences with our experts and these participants.
For More Information- https://www.globalcompliancepanel.com/control/sponsorship
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