Risk Management

Learn more about risk management, including ways to minimize, monitor, and control their impact.

  • Lessons Learned for Reducing Risk in Product Development43:42

    Lessons Learned for Reducing Risk in Product Development

    In this webinar, we’ll demonstrate how Jama Connect® creates Live Traceability™ through siloed development, test, and risk activities to effectively reduce risk in the product development process.

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  • Understanding Integrated Risk Management for Medical Devices

    Understanding Integrated Risk Management for Medical Devices

    In this paper, industry solution experts share best practices for integrated risk management, how to integrate risk-based thinking into product development cycles, and the importance of traceability.

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  • Understanding Integrated Risk Management for Medical Device1:02:57

    Understanding 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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  • Learn More About Requirements Management

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  • Learn the Essential Elements of a Successful Review Process

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  • Axendia Report: The Costly Impact of Ineffective Requirements Management

    Axendia Report: The Costly Impact of Ineffective Requirements Management

    In this medical device research study from Axendia, a leading Life-Sciences Analyst firm, see how ineffective requirements management can negatively impact budgets, traceability, and V&V activities.

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  • Why Move Away from IBM® DOORS® Legacy, and Why Now?: Part 2

    Why Move Away from IBM® DOORS® Legacy, and Why Now?: Part 2

    This is Part 2 of a series examining the role legacy requirements management solutions, such as IBM® DOORS®, play in introducing project risk to the product development process. To read Part 1, ...

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  • Jama Connect for Medical Device Development

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  • The Rapid Rise of Digital Health Technology: Challenges and Keys to Success

    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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  • Get Started
  • 3 Ways Requirements and Risk Management Continue After Market Launch

    3 Ways Requirements and Risk Management Continue After Market Launch

    Congratulations!  Your organization has gained regulatory approval and launched its medical device product.  The ‘History’ in Design History File may elicit impressions that all those design and...

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  • Tips to Manage Product Development Complexity and Traceability

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  • Why Startup Medical Device Companies Should Prioritize Requirements and Risk Management Before QMS

    Why Startup Medical Device Companies Should Prioritize Requirements and Risk Management Before QMS

    As a medical device product development consultant, I often see start-up companies having trouble deciding what to prioritize – design controls and risk management or the quality management system...

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  • With Jama Connect®, TELEDYNE e2v Improves Communication, Review Cycles, and Efficiencies, Reducing Risk in the Development Process

    With Jama Connect®, TELEDYNE e2v Improves Communication, Review Cycles, and Efficiencies, Reducing Risk in the Development Process

    In this post, we look at how Teledyne e2v leverages Jama Connect for improved communication and better risk management.  Teledyne e2v is a global leader in specialized components and subsystems...

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  • Frost & Sullivan - How Jama Helps Businesses Thrive in Regulated Industries

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  • Why Move Away from IBM® DOORS® Legacy, and Why Now?

    Why Move Away from IBM® DOORS® Legacy, and Why Now?

    In this paper, we examine the role legacy requirements management solutions play in introducing project risk to the product development process, and look at modern alternatives to IBM DOORS.

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  • Five Key Design Control Practices that Improve Compliance and Help Develop Better Products

    Five Key Design Control Practices that Improve Compliance and Help Develop Better Products

    Design Controls have been an FDA Quality System Regulation since 1997. Having worked on developing products in the regulated medical device industry for over 35 years, I have compiled a list of...

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  • magniX, Selects Jama Connect® for Its Ease of Use and Quick Deployment

    magniX, Selects Jama Connect® for Its Ease of Use and Quick Deployment

    In this customer story, we look at why magniX chose Jama Connect to help modernize their requirements management program and demonstrate compliance with standards.

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  • Jama Connect Ensures Requirements and Regulatory Compliance for Aerospace & Defense

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  • Regulatory Shift for Machine Learning in Software as a Medical Device (SaMD)

    Regulatory Shift for Machine Learning in Software as a Medical Device (SaMD)

    Machine Learning in Software as a Medical Device Machine learning (ML), a subset of artificial intelligence, has become integral across software in all industries, and the medical and life science...

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  • Buyer's Guide - Selecting a Collaborative Software Requirements Management Platform

    Buyer's Guide - Selecting a Collaborative Software Requirements Management Platform

    Download this eBook to see how software teams are using Jama Connect’s single requirements platform to accelerate time to market.

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  • Jama's Solution for the Automotive Industry

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  • Jama Connect Software Collaboration Datasheet

    Jama Connect Software Collaboration Datasheet

    Download this datasheet to see how software development teams are using Jama Connect’s single requirements platform to accelerate time to market.

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  • Jama Connect FMEA Framework for Automotive

    Jama Connect FMEA Framework for Automotive

    See how the Jama Connect® FMEA Framework assists automotive development teams when conducting comprehensive Failure Mode and Effects Analysis in this comprehensive datasheet.

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  • Watch Jama Connect's Test Management Platform in Action

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  • Reduce Project Risk in the Product Development Process

    Reduce Project Risk in the Product Development Process

    In this eBook, learn to reduce project risk in the development process by implementing Living Requirements™ management forming a digital thread through siloed development, test, and risk activities.

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  • 8 Do’s and Don’ts for Writing Requirements

    8 Do’s and Don’ts for Writing Requirements

    Every word matters when authoring requirements. In this post, we discuss the top dos – and don'ts – for successfully writing requirements.

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  • FREE GUIDE: How to Get the Most From a Requirements Management Platform

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  • Keeping Autonomous Vehicles on Track

    Keeping Autonomous Vehicles on Track

    Experts discuss actions engineers can take to stay nimble, innovative, and reduce safety-critical mistakes throughout the development process.

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  • Jama Connect® for Medical Device Startups Datasheet

    Jama Connect® for Medical Device Startups Datasheet

    In this datasheet, experts demonstrate how to leverage Jama Connect for Medical Device Startups to accelerate innovation while adhering to industry regulations.

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