Medical Device
Learn how Jama Connect for Medical Device Development can help teams demonstrate traceability, manage risk analysis, maintain audit trails, export data, streamline compliance and more!
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The Rapid Rise of Digital Health Technology: Challenges and Keys to Success
In this whitepaper, experts from Beanstock Ventures cover the emergence of Software as a Medical Device (SaMD), potential challenges for digital health technology, and recommendations to address them.
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Learn How Jama Accelerates Medical Device Development While Reducing Risk
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1:02:57WatchUnderstanding Integrated Risk Management for Medical Device
In this webinar, experts will walk through how to take a comprehensive and integrated approach to risk management for medical device development – and the benefits.
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FDA New Draft Guidance of Premarket Submissions for Medical Devices: Are you ready?
Learn about the new draft guidance for Premarket Submissions for Device Software Functions, the documentation levels, and the software documentation elements required for medical device development.
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Apex.AI Selects Jama Connect® to Shorten Development Time, Increase Efficiency, and Sail Through Audit Preparation
See how Jama Connect’s modern requirements management solution helps the innovative team at Apex.AI deliver safety-critical applications in automotive development.
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What the New Medical Device Regulations (EU MDR) Mean for You
The new Medical Device Regulation (EU MDR) addresses software as a medical device (SaMD), as well as other products. Here, we cover the new regulations and highlight the most important changes.
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54:38WatchComplying with FDA Design Control Requirements Using RM Principles
Join our webinar to learn more about how a good requirements management process helps facilitate compliance with FDA design control requirements.
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Jama Connect for Medical Device Development
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Medical Device Startup, Proprio, Chooses Jama Connect® to Drive Innovation
Read this customer story to learn more about the value of a requirements-driven product development process and the limitations of the typical Quality Management System (QMS).
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49:26WatchEnsuring FDA Compliance for Your Digital Health Solution
Attendees will hear directly from industry leaders Jama Software, MDM Engineering Consultants, & Beanstock Ventures about critical standards and best practices to follow in digital health development.
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Experience Jama Connect First Hand with a 30-Day Trial
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The Complete Guide to ISO 13485 for Medical Devices
Read this guide to learn the purpose of ISO 13485 and requirements for adherence, the difference between ISO 13485 and other medical device standards, and get key steps to adoption and certification.
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Jama Connect® for Medical Device Development Datasheet
Download this datasheet to learn how Jama Connect for Medical Device Development accelerates innovation in medical device development while adhering to industry regulations.
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ReadInfographic: Jama Connect™ for Medical Device Development
Infographic: Jama Connect™ for Medical Device Development We’re excited to share our latest infographic for the Jama Connect for Medical Device Development solution which explains how Jama Connect...
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Your Guide for Selecting a Medical Device Development Platform
Learn what to look for in a medical device development platform to help accelerate the development of safe, high-quality devices while managing ever-shifting complexities and regulations.
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Jama Connect for Medical Device Development
Learn how using a single platform can help accelerate innovation, maintain consistency and high product quality, and manage ever-changing complex regulations in medical device development.
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Application of Risk Analysis Techniques in Jama to Satisfy ISO 14971
Tips for Medical Device Companies, Interested in Risk Techniques following ISO 14971, ISO 13485, FMEA, FTA, and 21 CFR Part 820.
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10:22WatchJama Connect™ for Medical Device Development Demo
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The New EU In Vitro Diagnostic Regulation: What's Changing and What You Need to Know
In this whitepaper, we’ll discuss how emerging In-Vitro Diagnostics (IVDs) will be developed, managed, and regulated in the EU and beyond according to the new In Vitro Diagnostic Regulation (IVDR).
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32:56WatchDriving Business Outcomes with Jama Software’s Success Programs
In this webinar, learn more about how Jama Software has created specific diagnostic tools and solution offerings to achieve higher value with Jama Connect.
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ReadReclaiming Productive Work Time - ROI Calculator
Reclaim productive work time spent on manual activities, siloed data, sleuthing out change impact, etc. by implementing a modern requirements management solution into your development process.
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ReadReduce Rework - ROI Calculator
Use this handy ROI calculator to learn how much last-minute delays and rework is costing you and how much budget can be reclaimed with a modern requirements management solution like Jama Connect.
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30:57WatchImplementing Requirements Management for ISO 21434
In this webinar, experts discuss the emergence of cybersecurity concerns in the automotive industry, ISO 21434, and implementing a TARA in a requirements management database.
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