Authors


Ecolab

Latest:

Ecolab Continues Mission to Protect What's Vital With Deep Investment in Life Sciences

Ecolab is looking to the future with new opportunities to partner with Pharma for critical solutions to support drug development and manufacturing.


Chalana Damron

Latest:

PREP Act Protections for COVID-19 Vaccine Liability

How PREP Act protections will apply to potential COVID-19 vaccine-related claims.


Erin O'Hare

Latest:

Best Practices for Balancing Medical Affairs Globalization with Local Requirements

Addressing the challenges faced by Global Medical Affairs teams and how they can find balance to create maximum value for their organizations.


Corey Ford

Latest:

The IRA Impact: Navigating Its Evolving Complexities

Amid lingering questions and uncertainty, a look at ways pharma companies can prioritize incorporating the Inflation Reduction Act into their strategic planning process—and do it now.


Selene Peng

Latest:

China’s Trial Advantage: Tracking Nation’s Growth in Pharma Innovation and Global Investment

A look at China's emergence as a hub for novel treatment pursuits—and ways international investors can best capitalize on the favorable research trajectory.



Kevin L. Hagan

Latest:

The Quest to Fully Address Prescription Drug Affordability

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


Natalya Stone

Latest:

The JAKs Journey Offers Valuable Lessons for Innovators

Opportunity remains despite regulatory and access obstacles.


Jim Whitaker

Latest:

Why A New Mix of Field Skills is Crucial to Thriving in the Digital Era

Evolving preferences of HCPs during the pandemic have put an emphasis on learning new skillsets for pharma reps.


Dea Belazi

Latest:

SPBMs: Impact on Accessibility & Affordability of Gene Therapies for Rare and Orphan Diseases

The introduction of alternative payment models and specialty pharmacy benefit management (SPBM) is poised to usher in a new era of affordability for expensive gene therapies.


Michael O’Connor and Isha Arora

Latest:

The Department of Justice is Watching: Building a Data-Driven Compliance Program

Whether your company already has a data-driven compliance program in place or is contemplating building one, Michael O'Connor and Isha Arora outline four things the DOJ is now focused on that your compliance team needs to know.


Brent Herspiegel

Latest:

When to Utilize Commercial Outsourcing

When deciding on the right commercialization model, organizations must consider multiple factors, including the asset or platform they possess, the launch timing, the funding required, and staffing expertise.


Sachin Purwar

Latest:

Investing for Success: Finding the Right Launch Balance

Challenge assumptions and reset expectations when it comes to pre-launch SG&A investment to increase the odds of commercial success.



Andrew Cournoyer

Latest:

A Case for Payer Engagement and Participation in Clinical Research

Collaboration can make commercialization processes efficient and effective.


Vijesh Unnikrishnan and Ganesh Vedarajan

Latest:

The Teladoc-Livongo Merger: Life Science Manufacturers’ Darwinian Moment

The recent merger of Teledoc and Livongo into a $38 billion titan proves that the market sees opportunity in health tech. Could it be an inflection point in our race towards a digital-first care model, or is this an experiment ahead of its time?


Glen Pearce

Latest:

How Medical Affairs Can Contribute to Successful Drug Launch

Faster launch planning leads to greater access.


Lauren Nestor

Latest:

Navigating the Payer-Health System Nexus: A Strategic Imperative for Biopharma Commercial Success

The traditional biopharma approach focused primarily on physician detailing and securing favorable payer contracts, has become inadequate in today’s market.


Enoch Kariuki

Latest:

China: The Giant Has Awoken

With a new Chinese pharma or biotech company listing on either the HKEX or STAR exchange in China almost every week, it is important consideration US pharma and biotech companies to have a focused China market strategy, writes Enoch Kariuki.



Jonathan E. Levitt, Esq.

Latest:

The Consolidated Appropriations Act and PBM Transparency

New federal law introduces significant changes in the design of pharmacy benefit plans with aims to level the playing field between PBMs and their employee healthcare benefit plan clients.


John Reuter

Latest:

Embracing the Hybrid Era: Leveraging Answer Engines and Generative AI to Improve the Patient and HCP Experience

Through the power of large language models and generative AI, pharma and biotech companies are transforming medical information delivery by offering direct, trustworthy, and accurate answers to patients and healthcare providers, significantly reducing time and frustration.


Kerim Ozbilge

Latest:

Enhancing Supply Chain Resilience amid Complexity in Pharma and Medical Devices

The growing complexity of supply chains necessitates the adoption of collaborative planning processes and capabilities such as S&OP and S&OE.



Sheila Thorne

Latest:

The Cultural Deficit in the Pharma Industry in the Era of COVID-19

Multicultural campaigns crafted for diverse populations are insufficiently funded and do not receive the same support as mainstream campaigns, writes Sheila Thorne. While there are plenty of people willing to partner with pharma on these campaigns, will the industry wake up to the changing world ahead?



Morten Nielsen

Latest:

Measuring Pharma’s Trust Performance

The core building blocks of trust must be operationalized for pharma companies to strengthen their social contract, deliver business value, and improve patients’ quality of life.


Sandra Von Meier

Latest:

Advancing Healthcare Solutions: Harnessing Collaborative Business Models for Oncology

Unique approaches are needed to bring solutions to fighting cancer and bacterial-resistant infections.


Thomas Swalla

Latest:

Don’t Get Distracted By AI, Instead Focus on Intellectual Property

Artificial intelligence is making it quicker to get drug candidates to the clinic, but it isn’t addressing the fundamental need to marry the right candidate and the right target to the right disease.


Bryan McSwiney, Brand Insights Contributor, Global Director of Technical Operations for Zenith Technologies, a Cognizant Company

Latest:

How Life Sciences Can Move to Manufacturing 4.0 While Meeting Market Demands

Here are four ways life sciences organizations can quickly and cost-effectively achieve Manufacturing 4.0 benefits while still getting treatments to market.