HirLan, Inc specializes in the Integration of Products and Processes and are experts in the field of Product Design and Human Factors. HirLan can help with all aspects of the new FDA 510(k) Human Factors Guidance including Medical Device and Electronic Medical Records (EMR) Testing.
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HirLan, Inc. | hirlan.com Reviews
https://hirlan.com
HirLan, Inc specializes in the Integration of Products and Processes and are experts in the field of Product Design and Human Factors. HirLan can help with all aspects of the new FDA 510(k) Human Factors Guidance including Medical Device and Electronic Medical Records (EMR) Testing.
hirlan.com
HirLan, Inc.
http://www.hirlan.com/5_institute.html
HirLan Institute of Human Factors. Including Human Factors Research and Evaluation into the product lifecycle ensures that your products will be safe, effective and profitable. The HirLan Institute of Human Factors is dedicated to designing and evaluating products using the methods that are based in cognitive-behavioral psychology. Our experience spans the following product areas:. Transportation: aerospace, aviation, automotive and mass transit. Software: computer, smartphones, tablets and embedded.
HirLan, Inc.
http://www.hirlan.com/3_evaluation.html
Product validation, Human Factors Engineering and User Experience testing are all part of the User Centered Participatory Design process. With R&D expenses escalating, it is beneficial to limit and minimize product risk by identifying product flaws as early in the process as possible. Hirlan can help with:. In depth resources and training on the new FDA 510(k) Human Factors/Usability Requirements and Methods. How to integrated Human Factors methods and testing into your Product Life Cycle.
HirLan, Inc.
http://www.hirlan.com/2_smartdevices.html
Modern smart devices include smart phones, tablets, handheld inventory control devices, and GPS to name a few. The applications for these devices find themselves in the hands of just about any user, in every environment. HirLan is experienced in application design and application prototype for all of these smart devices:. Smart Phones and Tablets. IPhone, iPad, Android. Kiosks and Handheld Applications. Informational and Transactional Applications. 2006-2016 HirLan, Inc.
HirLan, Inc.
http://www.hirlan.com/4_overview.html
2006-2016 HirLan, Inc.
HirLan, Inc.
http://www.hirlan.com/3_process.html
Stakeholder participation in the. Ideation phase of product. Development is vital to success. HirLan uses IdeationTek to. Manage the ideation phase of. HirLan helps customers build products that meet user/customer needs and requirements; that meet federal and consumer requirements and that are profitable. The following business processes have been shown to result in profitable products:. Managing the Innovation Process. Stakeholder Participatory Decision Making. Human Factors Principles and Guidelines.
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Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/service.html
Call Us: (619) 301-2073. HirLan, Your Human Factors Partner. Our Key Methods include:. Iterative Design and Testing Methods. Human Factors Design Best Practices. User Centered Participatory Design Methods. Learn About Human Factors. 2006-2013 HirLan, Inc. Medical Device Human Factors is a service provided by HirLan, Inc.
Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/service_col.html
Call Us: (619) 301-2073. Collateral Development That Meets the FDA’s 510(k) and CE Mark Guidance. HirLan helps customers create, produce, evaluate, and validate all types of print, electronic and video product collateral meeting all ANSI/AAMI HE75:2009(R)2013 and IEC 62366-1:2015 Human Factors Requirements. HirLan’s principals actually contributed to the creation of the ANSI/AAMI HE75:2009(R)2013 and FDA 510(k) Human Factors Requirements so you can be assured your:. Information for Use (IFU).
Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/service_510.html
Call Us: (619) 301-2073. How FDA 510(k) Guidance affects. HirLan specializes in User Centered Design and the evaluation process associated with innovative ideas, product features, and the final integration of innovation and User Centered Design. HirLan can help you meet the new FDA 510(k) Human Factors requirements through the:. Integration of the FDA 510(k) Human Factors Guidance into your product lifecycles. Evaluation and Validation of your products against general Human Factors Principles.
Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/service_pro.html
Call Us: (619) 301-2073. Experts in Managing Human Factors. Throughout the Product Lifecycle. Managing the Innovation Process through effectively collecting and prioritizing Innovative Product Ideas, Requirements and Features. Software and Mobile Device Design Process Review. User Centered Participatory Design Process Seminars. Iterative User Centered Design. Stakeholder Participatory Decision Making. Usability Testing: Evaluation and Validation. Learn About Human Factors.
Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/service_testing.html
Call Us: (619) 301-2073. HirLan, Global Human Factors Testing Experts. Learn About Human Factors. 2006-2013 HirLan, Inc. Medical Device Human Factors is a service provided by HirLan, Inc.
Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/event_mtg.html
Call Us: (619) 301-2073. FDA 510(k) Human Factors Guidance. There has been a lot of talk and some confusion about implementing the FDA 510(k) Human Factors Guidance. Breakfast Meeting - La Jolla, CA March 13, 2013 8:00am. An Introduction to the FDA 510(k) Human Factors Guidance. Learn About Human Factors. 2006-2013 HirLan, Inc. Medical Device Human Factors is a service provided by HirLan, Inc.
Medical Device Human Factors by HirLan, Inc
http://www.medicaldevicehumanfactors.com/index.html
Call Us: (619) 301-2073. Are you wrestling with the new FDA 510(k) Human Factors Regulations? How are you accommodating the FDA 510(k) Human Factors guidance in your product design and management processes? Do you need help with the CE Mark? HirLan partners with medical device manufacturers to assist with Human Factors Engineering through product innovation, development, validation/evaluation testing, and delivery. Learn About Human Factors.
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HirLan, Inc.
Introducing: The HirLan Institute of Human Factors. Medical Devices and Software. Tools for Idea Management. Product Design Best Practices. Human Factors Life Cycle Processes. Evaluation and Validation Studies. FDA 510(k) Human Factors Guidance. Heuristic Evaluations, Focus Groups. New Ideas and features are the basis of business. How are you managing innovation? How are you deciding your next set of product features? HirLan products and services can help you through this process. 2006-2017 HirLan, Inc.
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