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Solutions

Solutions

Explore end-to-end solutions throughout development — from portfolio optimization and regulatory strategy, to Phase I-IV clinical trials, market access planning, and more.

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WHAT WE DO

  • Portfolio management and asset valuation
  • Early development and innovation
  • Integrated clinical development
  • Approval and access
  • Value substantiation lifecycle management

HOW WE DO IT

  • Delivery models
  • Operational excellence
  • Medical affairs
  • Portfolio management and asset valuation
    • Building patient insights into assets, profile and claims
    • Portfolio optimization
    • Asset valuation and indication prioritization
    • Early evidence review
    • Quantitative Clinical Pharmacology and Model-Informed Drug Development (MIDD)
    • Integrated development strategy and planning
  • Early development and innovation
    • Phase I Clinical Trials
    • Site Alliance Network and KOL Engagement
    • Regulatory Strategy
    • Real World Evidence
    • Market Access Strategy and Delivery
    • Biomarker and Genomic Medicine Strategy
    • Medical Communications
  • Integrated clinical development
    • Phase IIB-IV Clinical Trials
    • Real World Evidence
    • Quantitative Clinical Pharmacology and Model-Informed Drug Development (MIDD)
    • Protocol-Driven, Customized Site Solution Strategy
    • Patient Inclusion
    • Regulatory Strategy, Submissions, Compliance, and Outsourcing
    • Market Access Strategy and Delivery
    • Clinical Development Technology Optimization
    • Clinical Trial Supply & Logistics
    • Medical Communications
    • Drug Safety and Pharmacovigilance
  • Approval and access
    • Real World Evidence
    • Global Regulatory Submissions and Outsourcing
    • Compliance and Risk Management
    • Market Access Strategy and Delivery
    • Medical Communications
    • Drug Safety and Pharmacovigilance
    • Health economics modelling and simulation
  • Value substantiation lifecycle management
    • Real-World Evidence, Market Access Strategy and Planning
    • Regulatory Compliance
    • Lifecycle Optimization
    • Drug Safety and Pharmacovigilance
    • Medical Communications
  • FSP delivery models in clinical trials
    • Gain an advantage through FSP
  • Operational excellence
    • Leveraging AI in clinical development
  • Medical affairs for clinical trials
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Biotech

Get the personal, responsive, and committed approach of a small CRO, with all the benefits of a large CRO, to help you develop life-changing treatments for patients.

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Clinical Trialblazers Podcast

Step into the world of biotech leaders and hear the untold stories behind their journeys to bring breakthrough innovations to life.

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Therapeutic Expertise

Therapeutic Expertise

Utilize our expertise across therapeutic areas, combining innovative trial designs, leading clinical and regulatory expertise, global reach, and a passion for changing patient lives.

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Therapeutic Expertise

  • Neuroscience
  • General medicine
  • Infectious disease & vaccines
  • Inflammation & immunology
  • Oncology
  • Hematology

Cross-Therapeutic Expertise

  • Cell & gene therapies
  • Pediatrics
  • Rare diseases
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Insights

Insights

Our experts help you stay at the forefront of the industry - and ahead of change.

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New Medicines, Novel Insights

  • New frontiers in neuroscience
  • Precision oncology
  • Rare disease drug development
  • Cell and gene therapy development
  • Patient-guided drug development

Clinical Trialblazers Podcast

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Participate

Participate

Thinking about joining a clinical trial? Learn the drug development process, what it’s like to participate, how to find a trial, and answers to frequently asked questions.

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INTERESTED IN PARTICIPATING?

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HEAR FROM REAL PATIENTS

  • Patient stories

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Sites

Sites

Want to collaborate with us to offer clinical trials at your site? We would welcome the opportunity to discuss.

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About

We are one of the largest CROs in the world, speeding life-changing medicine to market by engaging patients With Heart™. Learn about who we are, what we do, and what we believe.

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