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September 26-28 | San Diego

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Content Library

  • Industry Survey TN

    PFS Survey Results

    We’ve recently conducted an industry-wide survey to understand how the community can accelerate injectable device developments.

    Survey respondents include both large pharma and small biotech organizations, spanning across departments from formulation to regulatory affairs, from device development to manufacturing.

    Take a look at what your peers think about the major hurdles and areas of most growth in this space.

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  • TN

    Past Presentation Pack

    Enjoy key insights on the following topics:

    Combination Products: Dealing with Global Regulations
    By John Smith, Director, Global, Regulatory Affairs, Allergan

    Device Requirements for Injection Devices to Safeguard Compliance in Global Regions
    By Gopi Vudathala, Head, Regulatory Affairs CMC & Compliance, GSK Vaccines

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  • Shannon Clark TN

    Why use-related risk for injectable devices is crucial?

    Enjoy this exclusive interview to gain key insights from Shannon Clark, CEO, UserWise, Inc., a specialist in human factors risk assessment and use-related risk analysis.

    It’s important to do a usability study as soon as a device is identified and developed – this helps you to recognize any design flaws that require improvement…save your organization a tremendous amount of effort, time and costs! 

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