Authors


Mariel Metcalfe

Latest:

Atopic Dermatitis — Going Beyond the Pill

There is a real opportunity for pharma to support the under-served population of atopic dermatitis patients, writes Mariel Metcalfe.



Maarten Beekman, MD

Latest:

Medical Affairs’ Search for Meaning

The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.


Alexander Bedenkov, MD, PhD

Latest:

Medical Affairs’ Search for Meaning

The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.


Filip Surmont, MD

Latest:

Medical Affairs’ Search for Meaning

The need to look beyond the function’s traditional performance measures to the one that really matters-patient outcomes.


Prashant Dhanavade

Latest:

ICH E2B (R3) EudraVigilance

Impact, challenges and the importance of ensuring readiness with ICH E2B (R3) EudraVigilance.


Graham Francis

Latest:

Establishing End-to-End Control of Product Labelling: A Guide for the C-Suite

Graham Francis sets out 5 critical business drivers for building a global enterprise labelling strategy over the year ahead.



Jeremy Schafer

Latest:

How Copay Management by Payers Is Evolving

A look into the complex battle between pharmaceutical manufacturers and payers for balance between medication access and budget management.


Kellie Rademacher

Latest:

The AI Boom in Healthcare: How Manufacturers Can Prepare

Kellie Rademacher identifies some of the key questions to consider when choosing an AI partner.


Stephen Ferrell

Latest:

Deploying the Cloud in GxP Environments

Meeting the stringent cloud compliance and regulatory requirements in pharma. 


Jaleel Shujath

Latest:

Productivity Vs. Compliance: The Balancing Act of ECM in Life Sciences

While digital transformation in life sciences starts with digitization for compliance, it should be seen as a key lever of competitive advantage and success, writes Jaleel Shujath.


Jack Barrette

Latest:

Patient KOLs: Their Guide to Entering Crowded Markets

How “patient influencers” look beyond price to help the industry evaluate newly-launched brands.


Michael Joachim

Latest:

Patient Empowerment and the Future of Pharma Advertising

With digitalization enabling patient engagement with their own health experience more than ever before, two critical elements will steer pharma’s advertising path.


Annalisa Jenkins, MBBS, FRCP

Latest:

Clinical Trials Don't Have to Cost Too Much or Take Too Long

A discussion of the cost and time put into clinical trials.


Gen Li, PhD, MBA

Latest:

Clinical Trials Don't Have to Cost Too Much or Take Too Long

A discussion of the cost and time put into clinical trials.


Stephen Arlington, PhD

Latest:

Clinical Trials Don't Have to Cost Too Much or Take Too Long

A discussion of the cost and time put into clinical trials.


Paul Chew, MD

Latest:

KOLs: An Endangered Buzzword

KOLs have traditionally exerted their influence through research and publication on drug safety and efficacy, but now share the stage with other important measures.


Ashley Slavik

Latest:

The GDPR: A Journey to Compliance

Ashley Slavic details how Veeva Systems prepared for the EU data protection regulation, and what others can learn from the experience


Keith Bailey

Latest:

How to Select the Right Consultant

A variety of consultant options are available to the pharma industry; this article is a 3-step guide to selecting the right consultant.


Douglas Bock

Latest:

How to Select the Right Consultant

A variety of consultant options are available to the pharma industry; this article is a 3-step guide to selecting the right consultant.



Ellen Coleman

Latest:

Patient Advocacy: an Overlooked Strategy for Achieving Equitable Market Success?

Ellen Coleman outlines the highlights of a recent webinar on ensuring that patient advocacy is a key element of a market access strategy.


Nobuko Kobayashi

Latest:

Japan: Balancing Cost and Innovation through Pricing

Global pharma companies and Japan can create a win-win situation through a new pricing mechanism, writes Nobuko Kobayashi.


Adrian Leibert

Latest:

Improving Regulatory Resource Management through Systematic Measurement

As submissions complexity intensifies, the key to better resource management is better measurement, writes Adrian Leibert.



Oracle Health Sciences

Latest:

2021 Research: The Impact of New Clinical Trial Approaches Adopted During Pandemic

***Live: Tuesday, October 26, 2021 at 11 EDT | 8am PDT | 5pm CEST | 4pm BST*** Oracle Health Sciences reveals new research conducted to understand the technology adaptations that were made to clinical trials during the pandemic, the effect of these adaptations, and the impact of these changes on the future of clinical trials.


Brian Kennedy

Latest:

Engaging with Stakeholders In the Information Age

With so much information readily available companies have lost a significant level of control over how and when details about their progress in drug development and planning related to approval, launch, and commercialization are disseminated.


Andrew Butcher

Latest:

Engaging with Stakeholders In the Information Age

With so much information readily available companies have lost a significant level of control over how and when details about their progress in drug development and planning related to approval, launch, and commercialization are disseminated.


Doug Caldwell

Latest:

Cloud Levels Playing Field for Emerging Life Sciences Companies

A discussion of the benefits that a cloud-based strategy has to offer.