Medical device manufacturers must consider the differences between a device used in a professional setting versus one used in the home. The users, environments and risks are quite different. This paper explores those variations and how testing helps you comply and capitalize on the fast-growing home healthcare opportunity. Please complete the form below to download […]
In this new report, we explore the cycling and performance characteristics of various-sized batteries under different conditions and highlight the performance of Resonetics lithium ion cells manufactured for implantable medical applications. Read now via the form below.
Medical device regulations continue to grow more complicated. For regulatory affairs departments to manage the ongoing challenges in workloads and regulator expectations, organizations are going to have to start planning for change. Learn Cook Medical’s and Exact Sciences’ top suggestions for tackling regulatory challenges and igniting changes needed within your organization, including: How to build […]
No connection? No problem! A research team was looking to utilize a real-time EDC system inside ORs and ICUs with little to no internet access. It takes practical insight, a custom-designed database, and an innovative eCRF to build a seamless solution. It Takes Avania. View the Case Study via the form below.
While the medtech industry takes strides towards digital technologies, many still rely on manually intensive and time-consuming processes. Learn how Alcon and Terumo utilized digitization, redesigning their systems to increase efficiency, accelerate cross-functional procedures, and support continuous global regulatory compliance, including: ● Creating a Single Source of Truth Across Departments ● Integrating Risk Management into […]
Clinical investigations must have specific strategies and practices to be successful. Understand how particular requirements for clinical investigations exist under the European Medical Device Regulation 2017/745 (MDR). This document details conducting a clinical investigation including the medical device manufacturer required resources. Download full document below.
Manufacturers navigate various challenges in meeting the regulatory requirements related to Class III and implantable devices. Learn about the Summary of Safety and Clinical Performance (SSCP), a European Medical Devices Regulation 2017/745 requirement for devices to meet performance, clinical, and safety standards related to the device’s purpose. Download full document below.
After the publication of Directive 2007/47/EC in 2007, manufacturers must follow additional and revised guidelines related to the technical documentation of clinic evaluations. Understand how the requirements affect the focus of clinical investigation and how manufacturers can understand the criteria operate in practice, specifically regarding clinical investigation scope and planning. Download full document below.
Recession. Inflation. Supply chain challenges. These are some of the headwinds facing medtech companies today. Through this industry report, we’ll explore strategic considerations for managing through and coming out on top. With so much out of your control, focus on what you can with supply chain, sales and marketing strategies. Download Now.
Learn how the experts launch their medical devices. Definitive Healthcare’s eBook cowritten by Carl Zeiss Meditec Inc. is packed with checklists and descriptions of all major pre-launch action items each team in your org needs to complete to successfully launch your device. Download Now.
Medical device certification relies on a higher level of documentation than most categories. It’s important — especially for start-up companies — to realize that a functional prototype is NOT sufficient to meet the full regulatory burden. This whitepaper outlines a few key reminders essential for any new device launch. Download the whitepaper now! […]