Slideshare - All Slideshows

This Stream includes parexel's latest Slideshares

  • Improving Processes for Temperature Traceability from Packaging to Patient

    Improving Processes for Temperature Traceability from Packaging to Patient

    Check out this presentation from PAREXEL Randomization and Trial Supply Experts to learn about temperature monitoring practices throughout the clinical trial supply chain, including: traditional tempe

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  • Life of a Biosimilar

    Life of a Biosimilar

    Check out this presentation from PAREXEL Consulting experts to learn about key regulatory processes affecting biosimilars development including an an overview of the 351(k) Pathway, FDA approvals and

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  • Effective Strategies for Successful Global Development

    Effective Strategies for Successful Global Development

    Learn how to leverage effective strategies for global drug development, including expedited regulatory pathways, personalized medicines and genomics. View the full presentation from PAREXEL Consulting

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  • Trends in Early Development

    Trends in Early Development

    PAREXEL Early Phase Clinical Research Services experts discuss developing trends in drug development including adaptive trials design, real-world data and biomarkers.

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  • Understanding Regulatory and Payer Requirements Throughout Commercialization

    Understanding Regulatory and Payer Requirements Throughout Commercialization

    Learn about regulator and payer evidence requirements as well as other key market access considerations in drug development. Read this presentation from PAREXEL Consulting experts.

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  • Innovative Pricing and Reimbursement Schemes - The Why, What, Which & How

    Innovative Pricing and Reimbursement Schemes - The Why, What, Which & How

    Learn about the need for innovation in global reimbursement mechanisms, the potential risks and benefits of implementation, and real world examples in a presentation by PAREXEL Access Consulting Exper

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  • Leveraging Imaging and Wearable Technology For Agile Clinical Trials

    Leveraging Imaging and Wearable Technology For Agile Clinical Trials

    Learn how to manage and overcome key challenges to deploying imaging and wearable technology effectively in clinical trials from PAREXEL Consulting experts.

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  • Effective Regulatory Strategies for China Market Entry

    Effective Regulatory Strategies for China Market Entry

    Learn about the impact of China 's regulatory reforms for companies conducting clinical research in the country from PAREXEL Consulting experts.

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  • Seamless Dataflow with a Clinical Metadata Repository

    Seamless Dataflow with a Clinical Metadata Repository

    Learn how PAREXEL's Clinical Metadata Repository can help improve the way you manage clinical trial data.

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  • FDA Initiatives Under The 21st Century Cures Act

    FDA Initiatives Under The 21st Century Cures Act

    Learn about FDA's priorities for implementing The 21st Century Cures Act and how they will impact clinical research from PAREXEL Consulting experts.

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  • Exploring Ways to Enhance Evidence Generation & Communication Planning

    Exploring Ways to Enhance Evidence Generation & Communication Planning

    PAREXEL experts explore key aspects of successful evidence generation and communication plans and how to apply them in your organization.

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  • Operational Aspects of Independent Reviews for Immune-Oncology Clinical Endpoints

    Operational Aspects of Independent Reviews for Immune-Oncology Clinical Endpoints

    PAREXEL Consulting experts detail operational aspects of independent reviews in the context of immunotherapy clinical trials.

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  • Development Considerations Comparing Major Markets Including US, EU, Japan and China

    Development Considerations Comparing Major Markets Including US, EU, Japan and China

    PAREXEL Consulting experts compare regulatory requirements in major drug development markets including the US, EU, Japan and China.

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  • Understanding Different Stakeholder Requirements Throughout Commercialization

    Understanding Different Stakeholder Requirements Throughout Commercialization

    Learn how to use Real World Evidence (RWE) to bridge the evidence gap between regulators and payers.

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  • RIM & IDMP Synergies

    RIM & IDMP Synergies

    View the presentation to learn about RIM & IDMP synergies.

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  • The Art and Science of Productive FDA Meetings

    The Art and Science of Productive FDA Meetings

    View the presentation to learn key strategies for optimizing meetings with the FDA.

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  • Generating Evidence to Drive Patient Access

    Generating Evidence to Drive Patient Access

    View this presentation to learn strategies for generating evidence that will help your product clear market access hurdles.

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  • RIM & IDMP Synergies

    RIM & IDMP Synergies

    View the presentation to learn about RIM & IDMP synergies.

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  • Regulatory Strategy In Emerging Markets

    Regulatory Strategy In Emerging Markets

    PAREXEL Principal Consultant Angela McGillivary discusses commercial considerations, clinical development, regulatory requirements, submission and post approval strategies in emerging markets

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  • Aligning on Patient Outcomes - How Market Dynamics Can Facilitate RWD Solutions

    Aligning on Patient Outcomes - How Market Dynamics Can Facilitate RWD Solutions

    PAREXEL's Michelle Hoiseth on how pharmas can leverage Real-World Data to help improve patient outcomes.

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