Market access and communications

  • EMA Guidance: Management of Clinical Trials - What it means for Patients?

    EMA Guidance: Management of Clinical Trials - What it means for Patients?

    A lay summary for patients participating in clinical trials

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  • Putting the Pandemic in Plain Language

    Putting the Pandemic in Plain Language

    The COVID-19 pandemic has brought many negative feelings to the forefront of our everyday lives, including anxiety, fear and social division, but what if we explored the new positive relationships...

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  • CAR-T: How far have we come and where are we going?

    CAR-T: How far have we come and where are we going?

    In this episode, Doug Olson, one of the first CAR-T patients treated on a clinical trial for CLL almost 10 years ago, details his experiences with this therapy in its earliest days....

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  • Rare Diseases: Aligning Expertise2:06

    Rare Diseases: Aligning Expertise

    See how Parexel are bringing together regulatory and market access experts to help companies developing rare and orphan disease products. Learn more about our Regulatory & Access Consulting Group: htt

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  • Parexel Regulatory & Access Overview Brochure

    Parexel Regulatory & Access Overview Brochure

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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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  • Press announcement: Parexel unveils combined Regulatory & Access consulting organization

    Press announcement: Parexel unveils combined Regulatory & Access consulting organization

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  • Interview with Paul Bridges, Head of R&A

    Interview with Paul Bridges, Head of R&A

    If regulatory and payer landscapes are so different, then why bring the two worlds together?

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  • Reimagining The Global Value Dossier - Part 6

    Reimagining The Global Value Dossier - Part 6

    A clear value strategy is key to the success of any product attempting to enter the healthcare market; defining the right strategy should lead to the perfect positioning for your product and...

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  • Commercial and Regulatory Strategy Considerations for Biotech

    Commercial and Regulatory Strategy Considerations for Biotech

    Many critical and innovative new therapies today, including those for rare and untreated diseases, are in the biotech pipeline. In fact, today biotech represents more than 80 percent of the...

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  • Use Real-World Evidence to Navigate From Regulatory Approval to Reimbursement Success

    Use Real-World Evidence to Navigate From Regulatory Approval to Reimbursement Success

    Use Real-World Evidence to Navigate From Regulatory Approval to Reimbursement Success

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  • How to align your market access activities with your product value strategy

    How to align your market access activities with your product value strategy

    The value strategy (also termed value story) for your product should act as the cornerstone for all market access activities.  The value strategy drives your market access planning, which...

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  • Reimagining the Global Value Dossier - Part 4

    Reimagining the Global Value Dossier - Part 4

    Health Technology Assessment (HTA) agencies are increasingly demanding the inclusion of patient-relevant data in submission dossiers. It is evident that there is an effort to ensure...

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  • Commercializing Gene and Cellular Therapy

    Commercializing Gene and Cellular Therapy

    Gene and cellular therapy manufacturing requires strict control in current Good Manufacturing Practice (cGMP) facilities.  Designing a facility or finding a contract manufacturer to meet the...

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  • Capturing the patient voice in market access communications

    Capturing the patient voice in market access communications

    Patients have unique perspectives on their conditions that, when incorporated into value communications, can provide an authenticity and salience which would otherwise be lacking. Who knows...

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  • Parexel Biotech: The value of patient-centric approaches - escaping the clinic4:24

    Parexel Biotech: The value of patient-centric approaches - escaping the clinic

    Parexel’s Rosamund Round, Director, Patient Innovation Center and Amy McKee, Vice President, Regulatory Consulting Services sit down with Monica Theis, a breast cancer survivor and two-time clinical t

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  • Strengthen Your Product Value Story One Phase At A Time

    Strengthen Your Product Value Story One Phase At A Time

    Find out how to plan evidence generation for your value story!

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  • Estimating the burden of salivary gland cancer in Nordic countries

    Estimating the burden of salivary gland cancer in Nordic countries

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  • Vaccine reimbursement trends and associated challenges in Europe

    Vaccine reimbursement trends and associated challenges in Europe

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  • Abbreviated HTA pathways, expediting patient access to novel treatments

    Abbreviated HTA pathways, expediting patient access to novel treatments

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