Authors


Dave Hanaman

Latest:

A Crossroads for the Digital Therapeutics Industry. Now is the Time to Act

Recent events can provide digital therapeutics companies with clear lessons for the future.


Michelle Marlborough

Latest:

Why Machine Learning's Potential in Pharma Relies on Its Transparency

Despite the rapid innovation of machine learning, correct protocols to ensure compliance and trustworthiness must be considered.


Joe Nipko

Latest:

Overcoming AI Bias Within Life Sciences

How to cultivate trust & connections in life sciences in a time of AI bias.


Veronica Sandoval, PhD

Latest:

Harnessing the Power of Communities to Combat Healthcare Inequities

Biopharma has a responsibility to meet patients where they are.


Dennis Fournogerakis

Latest:

To Reduce Commercial Risk for Orphan Drugs, Transform Forecasting

To successfully commercialize orphan drugs, companies need to set aside general medicine strategies and adopt a more granular approach to identifying and capitalizing on commercial opportunities.


Amy Morgan

Latest:

The Emergence of Commercial Health Insurances as an Access Route to the Chinese Market

Commercial Health Insurance may bring more opportunities for market access in China.


Chiraag Bhadana

Latest:

AI’s Promise in Delivering on Patient-Centricity

How pharmaceutical companies can utilize AI at key stages of the treatment journey to enhance patient-centric engagement by increasing empathy and humanity in patient interactions.


Sarah Murchison

Latest:

Startup Launch Guide: Avoiding 10 Common Pain Points

With opportunity and risk lurking in equal measure, today’s key considerations for biopharma startups when building their leadership teams and product go-to-market strategies are outlined.



Christian Hinneburg

Latest:

Strategic Decision-Making in Early-Stage Drug Development and Lifecycle Management to Maximize a Drug’s Lifetime Value

Presenting a structured, decision-making approach for executive management to make sound strategic decisions for drug development and life cycle management.


Sadik Kassim

Latest:

Three Key Steps to Unlocking mRNA’s Potential Beyond COVID-19

Improvements in R&D, manufacturing, and data sharing will extend platform’s reach.


Bioforumis

Latest:

Digital Medicine and Pharma: The Partnerships Bringing Together Molecule and Software

Pharmaceutical Executive, in collaboration with Biofourmis, organized a roundtable of experts from various groups to discuss how digital medicine and pharmaceuticals are changing the trajectory of what drug development and clinical care look like together, with an emphasis on partnerships within digital health.


Salesforce

Latest:

Transforming Healthcare Data to Precision Medicine

A modern healthcare ecosystem involves various stakeholders and many forms of complex data. Collaborations and a range of advanced approaches are essential to providing more uniform and complete healthcare to patients.


Genpact

Latest:

The future of life sciences and healthcare v2

Genpact’s latest report, Life Sciences and Healthcare in the Age of Instinct, explores three major trends shaping the future of healthcare.


Ailsa Budden

Latest:

No Half Measures: How Medical Affairs Can Maximize and Measure Value

Education and knowledge transfer must be prioritized for industry to see sizable improvement in medical affairs.


Amy Niles

Latest:

The Quest to Fully Address Prescription Drug Affordability

The Medicare Part D cap won’t solve need for financial assistance.



Adam Schoen, JD

Latest:

IP and Capital

Treat patents as strategic business assets and build an IP portfolio.


Dr. Ben Green

Latest:

The Rapid Growth of Remote Patient Monitoring Solutions Can Accelerate Decentralized Clinical Trials

Pharma companies and RPM manufacturers must work together to find solutions to make DCT more commonly available.


Dan Fitzgerald

Latest:

How Good is a Good Product Launch?

A fresh look at how industry benchmarks can help fortify new drug launches to overcome today’s new market-entry barriers and higher expectations.


Venkatraman “Bala” Balasubramanian, PhD

Latest:

Using GenAI as a Co-Pilot for Regulatory Intelligence

GenAI is on the precipice of breaking new ground in regulatory intelligence; making strategists more efficient by alleviating challenges, streamlining regulatory research and submission processes.


Dean Mastrojohn

Latest:

Silver Linings of a Global Health Crisis: A New Path Forward for Pharma Media Professionals

at some point, we won’t be seeing wall-to-wall COVID coverage anymore, but stories about the fallout. How can pharmaceutical brands prepare for what’s next?


Chad A. Landmon, JD

Latest:

IP and Collaboration

Fighting the pandemic with joint projects and IP sharing.


David Ehrlich

Latest:

Industry Predictions For 2023

Top industry experts weigh in on what the new year holds for the pharma industry.


Girisha Fernando

Latest:

Instead of Drug Spending Caps, Medicare Should Try Value-Based Contracting

New regulations may require regulators to explore new payment options.


Crosstree

Latest:

Precision & Specialty Medicine Clinical Trials

Precision & Specialty Medicines are driving changes in the pharma development industry. We explore the changes these paradigms are having on the clinical trial space.


Catherine Tak Piech

Latest:

Shining a Light on Rare Disease: Evidence Challenges and Solutions

Significant challenges still lie ahead, but several specialists and a plethora of new technologies are well positioned to gather and analyze the evidence needed for diagnosing and treating rare diseases, writes Catherine Tak Piech.


David Kreutter

Latest:

Competing in Commercial Pharmaceuticals: Get Formal and Familiar with Analytics

Exploring the importance of analytics as a means of staying competitive in the commercial pharmaceutical market.



Jim Williams

Latest:

Four Critical Considerations for Launching Digital Diagnostic Tools

Creating a digital diagnostic that is supplemental and strategic to a company’s therapeutic asset requires due diligence to monetize the digital health innovation, or at least ensure optionality through the product development cycle.