Global Reach & Global Expertise

  • COVID-19 HEALTH AUTHORITY UPDATES 18 DECEMBER 2020

    COVID-19 HEALTH AUTHORITY UPDATES 18 DECEMBER 2020

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  • Parexel Biotech Brochure

    Parexel Biotech Brochure

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  • Case Study Achieving Product Endorsement after a FDA Warning Letter

    Case Study Achieving Product Endorsement after a FDA Warning Letter

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  • EU Clinical Trial Regulation 536/2014 Factsheet

    EU Clinical Trial Regulation 536/2014 Factsheet

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  • Top 10 Myths About Working with the FDA for an Oncology Drug Approval

    Top 10 Myths About Working with the FDA for an Oncology Drug Approval

    Amy McKee, Vice President Regulatory Consulting Services, addresses some of the most common misconceptions about working with the FDA.

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  • Perspectives on Three Recent Policies for Alcohol-Based Hand Sanitizer for Manufacturers during COVID-19

    Perspectives on Three Recent Policies for Alcohol-Based Hand Sanitizer for Manufacturers during COVID-19

    The COVID-19 pandemic has seriously impacted the US healthcare system and supportive manufacturing facilities. Some consumers and healthcare professionals are currently experiencing difficulties...

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  • How the UK's HTA Agency Uses Real-World Evidence to Develop Guidance

    How the UK's HTA Agency Uses Real-World Evidence to Develop Guidance

    The UK national health technology assessment (HTA) body, the National Institute for Health and Clinical Excellence (NICE), made a long-awaited announcement last week: NICE has expanded the...

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  • Commercial and regulatory strategy considerations for biotech

    Commercial and regulatory strategy considerations for biotech

    In this blog, Parexel regulatory and strategy experts tackle the question of how we can ensure that worthy innovations in the biotech pipeline make it to patients sooner.

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  • Regulatory Consulting Brochure

    Regulatory Consulting Brochure

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  • Unlocking the China Potential - Shamim Chowdhury1:52

    Unlocking the China Potential - Shamim Chowdhury

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  • Plan & engage early to manage the risks of risk management

    Plan & engage early to manage the risks of risk management

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  • Improving Drug Development & Patient Access With the Right People, Processes, and Culture

    Improving Drug Development & Patient Access With the Right People, Processes, and Culture

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  • What To Consider When Mapping Your Strategy For Submitting An Application To The National Drug Administration of China

    What To Consider When Mapping Your Strategy For Submitting An Application To The National Drug Administration of China

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  • Brochure: Regulatory, Development and Commercial Expertise. Operational Excellence. One Source.

    Brochure: Regulatory, Development and Commercial Expertise. Operational Excellence. One Source.

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  • Patient Recruitment in Asia

    Patient Recruitment in Asia

    Learn about patient recruitment strategies in Asia that will reduce the clinical trial burden, as published in Pharma Focus Asia in January 2018.

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  • Global Data Operations Overview Brochure

    Global Data Operations Overview Brochure

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  • Strategies for Working with Global Regulatory Agencies

    Strategies for Working with Global Regulatory Agencies

    It’s never too early to start crafting a global regulatory submissions strategy.

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