Regulatory Operations

  • Will You “Lose” On The FDAs 15 Day 483 Diet Plan?

    Will You “Lose” On The FDAs 15 Day 483 Diet Plan?

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  • Leveraging The Cloud To Accelerate Time To Treatment

    Leveraging The Cloud To Accelerate Time To Treatment

    Through a shared data platform built on a cloud computing model PAREXEL can enable efficiencies while also addressing the significant privacy, security and compliance challenges that the pharmaceutica

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  • Are You Keeping Pace with Digital Evolution?

    Are You Keeping Pace with Digital Evolution?

    As drug development timelines increase and access to data becomes even greater than ever, how is the industry utilizing digital technologies to make for a better future?

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  • See What Liquent InSight® Can Do For You

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  • DataLabs Designer Overview Factsheet

    DataLabs Designer Overview Factsheet

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  • Datalabs EDC Overview Factsheet

    Datalabs EDC Overview Factsheet

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  • Regulatory and Clinical Solutions Overview_APR18

    Regulatory and Clinical Solutions Overview_APR18

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  • You Have To Anyway! How and Why to Leverage IDMP Compliance1:00:12

    You Have To Anyway! How and Why to Leverage IDMP Compliance

    IDMP Compliance webinar delivered Dec. 6, 2016

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  • Avoid Approval Delays! FDA’s New Draft Good ANDA Submissions Guidance provides a “Must-Have List” of Common Deficiencies

    Avoid Approval Delays! FDA’s New Draft Good ANDA Submissions Guidance provides a “Must-Have List” of Common Deficiencies

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  • Aligning Clinical And Regulatory Functions - Part 2

    Aligning Clinical And Regulatory Functions - Part 2

    Instead of existing in silos, documents can be managed in a single repository

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  • Informa eRegulatory Summit

    Informa eRegulatory Summit

    Visit PAREXEL April 24, 2018 - April 26, 2018 Lisbon, Portugal

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  • PAREXEL Informatics: Decoding Data into Insights2:31

    PAREXEL Informatics: Decoding Data into Insights

    PAREXEL® Informatics is at the forefront of innovation and driving evolution by looking at technology and data differently. Our breadth and depth of expertise partnered with modern technology means we

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  • IMPACT® CTMS
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  • Optimize Your Regulatory Environment In 5 Simple Steps

    Optimize Your Regulatory Environment In 5 Simple Steps

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  • Transforming Clinical Trials: Reducing time to market

    Transforming Clinical Trials: Reducing time to market

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  • Strategies for Working with GRAs

    Strategies for Working with GRAs

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  • Intelligent Clinical Trials: How Technology Will Transform Clinical Trials57:29

    Intelligent Clinical Trials: How Technology Will Transform Clinical Trials

    How Technology Will Transform Clinical Trials To Lower Costs, Reduce Time To Market And Provide Value To The Patient.

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  • #DIA2018 | Microsoft's Desmond Creary on how Savings from Innovation Can Fuel R&D1:08

    #DIA2018 | Microsoft's Desmond Creary on how Savings from Innovation Can Fuel R&D

    From the floor at #DIA2018 - Microsoft Health Leader Desmond Creary explores how savings from innovation can help fuel greater R&D investment.

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  • Getting to Approval Faster Through Technology Innovation51:38

    Getting to Approval Faster Through Technology Innovation

    PAREXEL's Matt Neal joins experts from Microsoft and Allergan to discuss how innovations in technology can help patients by reducing the time and expense of bringing life-saving treatments to market.

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  • Regulatory Focus - Regulatory Challenges for Direct to Patient Studies

    Regulatory Focus - Regulatory Challenges for Direct to Patient Studies

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