Authors


Victoria Allan

Latest:

Why Is It Such a Challenge to Treat PAH?

Despite recent advances, there continue to be significant issues that compromise the effective management of pulmonary arterial hypertension, writes Victoria Allan.


Pharmaceutical Executive Editorial Staff

Latest:

Divergent Paths: Pharm Exec Profiles Five Recent Drug Launches

Pharm Exec’s latest sampling of notable biopharma brand approvals and launches all have unique stories to tell—from the winding journeys to innovative “firsts” to new momentum for milestones to come.


Arthur G. Cook

Latest:

The Challenge of Forecasting Biosimilars

The biosimilars market forecaster must create a framework that captures the dynamics that operate in these markets and do justice to the uncertainty and quantification of assumptions, writes Arthur G. Cook


Sarah Chaney

Latest:

The Salix-Valeant Acquisition: "It’s Just a Game"

Sarah Chaney gives an in-depth look at the Salix-Valeant acquisition - how analysts and investors can affect decision-making and potentially drive poor behavior.


WestRock

Latest:

Patient-centric innovation in packaging moves beyond regulatory requirements to deliver brand differentiation and increased sales

Not so long ago, pharmaceutical brand managers considered drug packaging an afterthought. Today, packaging not only matters, it is quickly becoming one of the most important considerations in the growth and success of any drug product. Manufacturers now consider innovative, smart packaging that pleases patients in their new roles as consumers, and encourages brand loyalty to be a game changer in an increasingly competitive and crowded biopharmaceutical market.


Sophie Daniel

Latest:

Europe Needs News Timeline for IDMP Implementation

All indications are that the July 2016 deadline for transition from Europe's eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) to the new Identification of Medicinal Products (IDMP) is not achievable. Sophie Daniels reports.


Kathleen Iacocca, Yao Zhao

Latest:

Resell vs. Direct Models: US Branded Drug Distribution in the Future

Kathleen Iacocca and Yao Zhao discuss why direct supply chain models can be more sustainable than resell models in the long run and whether they can be implemented in the US.



Stacie Heller

Latest:

New Payment Models: It's Time to Move

Commercial success for pharma brands now demands proactive strategies and interventions


Peter Weissberg

Latest:

New Payment Models: It's Time to Move

Commercial success for pharma brands now demands proactive strategies and interventions




Mara Senn

Latest:

Stop Everything! Investigating FCPA Issues in Pharma

An internal audit of payment practices in Eastern Europe has revealed payments for elaborate travel for government health authorities and state-employed physicians in exchange for approval and prescription of your products. What is the first thing you should do? Lawyer Mara Senn offers some advice.


Rik van Mol

Latest:

How eTMFs Are Transforming the Pharma Industry

A significant change is under way as the industry shifts from passive to active trial master file (TMF) management, writes Rik van Mol.


Ram Subramanian

Latest:

The Dawn of the Age of Value Pricing in Cancer?

What will the ASCO Value Framework mean for the industry? Ram Subramanian from Simon-Kucher & Partners gives six items to think about.


Stephen E. Littlejohn

Latest:

Walgreens: Purveyor or Provider?

The merger announcement from Walgreens Boots Alliance and Rite Aid throws up an interesting question, writes Stephen Littlejohn. Will Walgreens be purveyor focused on retail sales or provider engaged with a transforming U.S. healthcare system?


Mindy Ehrenfried

Latest:

Biosimilar Litigation: Lessons So Far

The case of Amgen v. Sandoz signals that preliminary injunctions will play major role in future patent disputes


William Raich

Latest:

Biosimilar Litigation: Lessons So Far

The case of Amgen v. Sandoz signals that preliminary injunctions will play major role in future patent disputes



Lev Gerlovin

Latest:

Restricted Access Essentials for Pharma

Where is US payer formulary management heading-and what can the industry do to help influence its course?


Michael Ricks

Latest:

Open Payments: Key Compliance Considerations

On June 30, the Centers for Medicare and Medicaid Services (CMS) released the first full year of data under The Affordable Care Act’s transparency program, also known as Open Payments or the "Sunshine Act." This included approximately 11.4 million records totaling about $6.5 billion in payments made to 607,000 physicians and 1,121 teaching hospitals by 1,444 reporting entities during 2014. Combined with CMS’s September 2014 release of 2013 data for the period Aug. 1, 2013 through Dec.


David Bennett

Latest:

Digital Integration Streamlining the Delivery of Compliant Promotional Content

By implementing integrated content compliance and digital asset management solutions into marketing workflows, life sciences companies can maximize the time and resources, writes David Bennett.


Peter Friedman

Latest:

Pharma’s Prescription for Social ROI

Measurement is a given in the pharmaceutical industry: dosage charts, chemistry formulas, budgets for testing, and budgets to go to market. When it comes to marketing, particularly through social media channels, measurement of return on investment (ROI) poses its own set of challenges. 


Pharmaceutical Executive Editors

Latest:

Pharmaceutical Executive's 2023 Emerging Pharma Leaders

Pharm Exec profiles its 2023 Emerging Pharma Leaders.


Susan J. Schniepp

Latest:

Biopharma: The Elements of Training

Establishing a well-defined training program is a crucial activity for any biopharmaceutical organization, writes Susan J. Schniepp.



John Swen

Latest:

Specialty Care Medicines: Managing the Impact of US Health Reform

There's been much talk of how US health reform will impact physicians, patients, and insurance companies. But how will it affect the often overlooked specialty drug market?



Rob Fox

Latest:

Expanded Access: Get Ready

While the initiation and management of an access program can be challenging and requires careful assessment and planning, the benefits to patients, healthcare providers and sponsoring companies are immeasurable, writes Rob Fox. “Patients will find you.”In his keynote address at this year’s World Orphan Drug Congress, Henri Termeer, the former CEO, chairman and president of Genzyme reminded the audience that patients will actively seek out companies developing new therapeutics for their unmet medical needs.


Thomas Hein

Latest:

Tablet Innovation: Sizing up the Value

The rising focus on difficulties in swallowing tablets spells a big opportunity for pharma.