Value Genome LLC
Value Genome LLC
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  • What We Do
  • WHO WE ARE
    • THE TEAM
  • Our Services
    • Market Access
    • HEOR / RWE
    • Medical Affairs
    • Patient Advocacy
  • CASE STUDIES
  • Contact Us

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Patient Advocacy: Enhancing Optimal Patient Health Outcomes

Empowering Patients, Optimizing Health Outcomes

Amplifying the Patient’s Voice with Business Understanding and Compassion

Amplifying the Patient’s Voice with Business Understanding and Compassion

With our Patient Advocacy Expertise, we ensure patients have rapid and unrestricted access to innovative therapy solutions. Value Genome partners with Life Science Companies and Patient Organizations to enhance patient health outcomes through dedicated advocacy services. 




Our deep understanding of Healthcare Law, the changing healthcare landscape and patients' hopes, desires and needs allows us to bridge the market access gap between innovative therapies and the individuals who can benefit the most from them. By placing patient’s wellbeing at the core of our market access efforts, we support life science companies in delivering not just innovative therapies, but comprehensive care solutions.

Amplifying the Patient’s Voice with Business Understanding and Compassion

Amplifying the Patient’s Voice with Business Understanding and Compassion

Amplifying the Patient’s Voice with Business Understanding and Compassion

We help both innovators and patient groups set priorities, focus energy and resources, strengthen operations, ensure that employees, volunteers and other stakeholders are working toward common goals, establishing agreement around intended outcomes/results and assess and adjust the organizations’ direction in response to a changing payer environment.


We infuse the patient’s voice into evidence generation and clinical trial planning. We guide patient groups and innovators through the entire FDA approval process, from preplanning strategy to market access. This includes ensuring the patient’s perspective is integrated into clinical trial design, regulatory submissions, and post-approval strategies, guaranteeing that therapies meet the highest standards of safety and efficacy while being accessible to those who need them most.

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