AHLA
Has your hospital or AMC considered using 3D printed devices in patient care? What are the regulatory considerations? Does the AMC become a manufacturer if it creates and uses a 3D printed device? What risks does the AMC taking on when manufacturing and using a 3D printed device. What contracts will be in place? Does the AMC need to purchase product liability insurance? This webinar will provide an overview of the regulatory, contractual and risk considerations when a provider manufactures and/or uses a 3D printed device.
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FDA issuance of the new Quality Management System Regulation (QMSR) to industry is meant to harmonize the current Quality System Regulation (QSR) for medical devices (21 CFR 820) with an incorporation by reference (IBR) to the 2016 edition of ISO 13485.
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Maria Whitman talks with Dr. Shantanu Nundy, M.D., MBA, about how the healthcare system needs to change to build trust and provide the best care. Dr. Nundy's perspective is informed by his work as a primary care physician and chief medical officer for Accolade, Inc.,
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modern healthcare
As more and more providers take action to adapt to a new era of value-based care, standardization has become an important priority to reduce clinical variation and ultimately improve outcomes. In order to do that, health systems have to make sure their providers are aligned with current evidence-based best practices, clinical guidelines and protocols. This webinar will discuss the significance of clinical reference resources in driving standardization, and explore how healthcare leaders are ensuring clinicians are equipped to provide high-quality, standardized care.
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