Value-Based Care

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Vtama Shows Strong Efficacy and Safety Even in Patients With Comorbidities: Druhan Howell, MD
0:26
Vtama Shows Strong Efficacy and Safety Even in Patients With Comorbidities: Druhan Howell, MD
4 days ago
by
Sabrina McCrear(+1 more)
Most Favored Nation Pricing Explained: Eleanor Perfetto, PhD, MS
1:08
Most Favored Nation Pricing Explained: Eleanor Perfetto, PhD, MS
7 days ago
by
Maggie L. Shaw(+1 more)
Poverty Stops Patients From Getting Chemo Even After Diagnosis: Lingling Du, MD
0:28
Poverty Stops Patients From Getting Chemo Even After Diagnosis: Lingling Du, MD
10 days ago
by
Sabrina McCrear(+1 more)
Why Clinical Trials Fail to Reach Many Racial Groups: Gen Li, PhD
0:45
Why Clinical Trials Fail to Reach Many Racial Groups: Gen Li, PhD
a month ago
by
Sabrina McCrear(+1 more)
Why Digital Control Arms Will Revolutionize Clinical Trials: Gen Li, PhD
0:36
Why Digital Control Arms Will Revolutionize Clinical Trials: Gen Li, PhD
a month ago
by
Sabrina McCrear(+1 more)
Why Breast Cancer Research Dominates Clinical Innovation: Gen Li, PhD
0:46
Why Breast Cancer Research Dominates Clinical Innovation: Gen Li, PhD
a month ago
by
Sabrina McCrear(+1 more)
Dr Ryan Haumschild
1:28
Value-Based Care, Infrastructure Drive Access to Disease-Modifying Therapies: Ryan Haumschild, PharmD, MS, MBA, CPEL
2 months ago
by
Brooke McCormick(+1 more)

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Clayton Irvine, PharmD, MBA, MS

Clayton Irvine, PharmD, MBA, MS, emphasized that optimizing value-based access to cell and gene therapies requires standardized care protocols, coordinated transitions between care settings, careful evaluation of prior authorization and financial assistance options, and formulary decisions that balance clinical outcomes with both direct and indirect costs to patients and institutions.

Jason Bergsbaken, PharmD, MBA, BCOP, explains the value of pharmacist involvement in precision molecular tumor boards and end-of-life care discussions, highlighting their role in ensuring evidence-based therapy selection, patient-specific recommendations, and shared decision-making that aligns treatment with individual goals.

Clayton Irvine, PharmD, MBA, MS, discusses strategies to address payer-driven biosimilar and prior authorization challenges through integrated digital solutions, while advocating for flexible, regularly reviewed treatment pathways supported by molecular tumor boards and artificial intelligence to balance standardization with personalized, biomarker-driven oncology care.

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