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Steam Sterilization in Health Care Facilities: A Review of ANSI/AAMI ST79:2017 (Webinar On Demand)

This webinar, led by two ST79 committee members, will discuss the process used to update ST79 and identify new and modified material in ST79:2017.
AAMI Member:
$20.00
List Price:
$35.00
Your Price:
$35.00
Available for Immediate Download
↑/↓ Full Details


Strategies to Conduct High-Integrity Validation Usability Tests

During this webinar, the presenters will review the myriad ways a validation test could be biased and ways to avoid it, thereby serving in the best interests of the manufacturer.
AAMI Member:
$135.00
List Price:
$225.00
Your Price:
$225.00
Available for Immediate Download
↑/↓ Full Details


Testing Training: Taking the Training Wheels Off

This webinar, referencing AAMI TIR49:2013, Design of training and instructional materials for medical devices used in non-clinical environments, will address ten of the most common questions related to training.
AAMI Member:
$135.00
List Price:
$225.00
Your Price:
$225.00
Available for Immediate Download
↑/↓ Full Details


The Benefits of UDI for Healthcare Technology Management

This webinar addresses the benefits of Unique Device Identification (UDI), UDI requirements in the U.S., challenges healthcare facilities are facing with UDI implementation, and the overall impact to quality and quality systems for both manufacturers and healthcare facilities.
AAMI Member:
$0.00
List Price:
$85.00
Your Price:
$85.00
Available for Immediate Download
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The Future Direction of HFE in Medical Device Development

This presentation will consider how trends in industrial, scientific, business, and consumer product and development might drive the design of future medical products.
AAMI Member:
$135.00
List Price:
$245.00
Your Price:
$245.00
Available for Immediate Download
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The Future of Healthcare Technology Management Webina

Paul Kelley presents this streaming webinar archive on the future of healthcare technology management. Specifically, Paul shares outcomes of the recent Future Forum on Technology Management, which include a recommendation on a new, unified name for the profession, as well as a desired future for the profession. Medical technology is evolving at such a rapid pace that the future of the profession is destined to change. The Future Forum created a roadmap for harnessing that change for the betterment of the profession.
AAMI Member:
$0.00
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$0.00
Your Price:
$0.00
Available for Immediate Download
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Understanding and Benefiting from AAMI/IEC 80001-1

This webinar will help suppliers of medical devices, IT technology, and telecommunications understand the standard ANSI/AAMI/IEC 80001-1:2010.
AAMI Member:
$0.00
List Price:
$85.00
Your Price:
$85.00
Available for Immediate Download
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Updates on AAMI ST79 and SPD Accreditation Surveys

This presentation is intended to help healthcare professionals prepare for a Joint Commission or Centers for Medicare and Medicaid Services survey as it relates to sterile processing of surgical instruments and other medical devices. We will discuss some of the recent updates to AAMI standards.
AAMI Member:
$20.00
List Price:
$35.00
Your Price:
$35.00
Available for Immediate Download
↑/↓ Full Details


Validation of a Medical Device Cleaning Process

There is increased focus by regulators around the world on medical device cleaning processes, and many medical device manufacturers find it a considerable challenge to plan and conduct a cleaning validation. The main challenges are an establishment of the cleanliness limits and an identification of the challenge conditions to be assessed during the process validation. This webinar describes logical and risk-based approaches to overcome these challenges.
AAMI Member:
$149.00
List Price:
$249.00
Your Price:
$249.00
Available for Immediate Download
↑/↓ Full Details


Warnings and Safety Information in Device Labeling

While most companies would readily acknowledge the importance of identifying and clearly communicating the potential hazards associated with their devices, oftentimes they are perplexed about the best methods for accomplishing it. Unfortunately, there is a dearth of actionable resources on how to design and develop warnings and safety information that stakeholders can readily access. This two-part series will address this gap.
AAMI Member:
$135.00
List Price:
$225.00
Your Price:
$225.00
Available for Immediate Download
↑/↓ Full Details


Webinar: HTM in a Box Orientation

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Learn all about AAMI's new "HTM in a Box" resource for promoting the HTM field. During this presentation, listeners will be guided through the three, age specific presentations about the HTM Field and learn about the other tools within the virtual box. Let's  work together to get the word out to everyone about how great our profession is!

Date:
Thursday, November 21, 2019
Time:
12:00 AM - 12:00 AM Eastern Standard Time
AAMI Member
$0.00
List Price
$0.00


Webinar: Stepping Through the New Environment on Imaging QA and TJC Requirements

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Description: Want to learn a best practice for meeting the imaging quality and regulatory requirements? Come hear a review of one organization’s efforts at complying with the new The Joint Commission requirements for fluoroscopy standards.

Date:
Tuesday, December 17, 2019
Time:
12:30 PM - 1:30 PM Eastern Standard Time
AAMI Member
$0.00
List Price
$0.00


Webinar: The Making of A Great BMET: Military Edition

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Description: This presentation is about what its like to go through the BMET School House at Fort Sam in Houston. The webinar will explain how to get into the program, opportunities for after a BMET successfully completes the program, and what career paths this program can lead to. The presentation includes after graduation tips and tricks to help a military BMET succeed as a civilian HTM Professional.

Date:
Tuesday, November 12, 2019
Time:
2:00 PM - 3:00 PM Eastern Standard Time
AAMI Member
$0.00
List Price
$0.00


Writing a Human Factors Engineering (HFE) Report

In 2011, the U.S. Food and Drug Administration (FDA) released a draft guidance document, Applying Human Factors and Usability Engineering to Optimize Medical Device Design, and this guidance calls for medical device manufacturers to include an HFE report when they apply for a 510(k) or PMA. The FDA goes so far as to provide a relatively detailed outline for the HFE report. However, many manufacturers are likely to have persisting questions about how to write an effective report.
AAMI Member:
$135.00
List Price:
$225.00
Your Price:
$225.00
Available for Immediate Download
↑/↓ Full Details


Writing an Effective Human Factors Engineering Procedure

This webinar discusses the need for medical device companies to create a human factors engineering (HFE) procedure that conforms to current HFE standards as well as the standards and expectations of the FDA and other regulators. Learn how an HFE procedure must be closely tied to a company’s risk management process (e.g., ISO 14971) and ways to turn a general procedure into a detailed and properly scaled one to guide a particular product development effort. This webinar serves the remedial benefit of explaining the purpose of the myriad HFE activities comprising a complete procedure. This webinar will enable audience members to immediately prepare appropriate procedures for their own organization.
AAMI Member:
$135.00
List Price:
$225.00
Your Price:
$225.00
Available for Immediate Download
↑/↓ Full Details


Writing Human Factors Plans and Reports Webinar

This webinar will fill a perceived gap in the guidance available to medical technology developers with sample work products and supplemental job aids that offer document preparation advice and have been peer-reviewed by a panel of HFE experts.
AAMI Member:
$149.00
List Price:
$249.00
Your Price:
$249.00
Available for Immediate Download
↑/↓ Full Details