Authors


Amber Gilbert

Latest:

Are Pharma Marketers Fighting the Last War?

Despite being the fastest growing influencers in healthcare, ad campaigns targeted at payers are often an afterthought.


Bob Ward

Latest:

Cystic Fibrosis: The Importance of Patient Advocacy

The importance of patient advocacy in boosting research for cystic fibrosis.


Justin Grossman

Latest:

Three Tips to Managing Multiple Agency Partners

Outlining three practices that are key to navigating today’s multiplayer agency landscape - and getting more value from each external vendor.


John Elliott

Latest:

The Path to Patient-Focused Accountability

Benchmark survey assesses the industry’s progress so far in moving from words to action in its approach to patient centricity.


Susan Darrah-Reilly

Latest:

Patient Support Programs: Cost, Benefit, and Resourcing

Working group explores the challenges of patient support programs (PSPs) and market research programs (MRPs) for pharmacovigilance (PV) professionals-and solutions currently being put into practice.


Tyla Sosa Hager

Latest:

Patient Support Programs: Cost, Benefit, and Resourcing

Working group explores the challenges of patient support programs (PSPs) and market research programs (MRPs) for pharmacovigilance (PV) professionals-and solutions currently being put into practice.


Louise Jebson

Latest:

Patient Support Programs: Cost, Benefit, and Resourcing

Working group explores the challenges of patient support programs (PSPs) and market research programs (MRPs) for pharmacovigilance (PV) professionals-and solutions currently being put into practice.


Daniil Graborov

Latest:

FDA Modernizes Controlled Correspondence Interactions with Pharma Industry

As part of FDA’s ongoing effort to modernize interactions with industry, FDA launched a portal to help with submissions of controlled correspondence via email instead of manual data entry.


Saundra Middleton

Latest:

FDA Modernizes Controlled Correspondence Interactions with Pharma Industry

As part of FDA’s ongoing effort to modernize interactions with industry, FDA launched a portal to help with submissions of controlled correspondence via email instead of manual data entry.


Alexis Normand

Latest:

How Blockchain Can Support FDA’s Agenda

The digitization of healthcare is paving the way to accelerate drug development in the industry, and the FDA is doing its best to support industry.


Partha S. Anbil

Latest:

Pharma's Incentive Compensation Plan Landscape

As pharmaceutical companies become increasingly focused on retaining key sales people, they continually consider ways to leverage variable compensation as a strategic tool for maximizing the return on their investment in top talent.


Tom Norton

Latest:

“Drug Transparency”: Each Bill Needs Careful Evaluation

Could the new Vermont Drug Transparency law “lead the US Pharmaceutical industry to an awful end”? Tom Norton reports.


Michael Jewell

Latest:

M&A: Range of Fundamental Factors Will Drive Strong Deal Flow

The outlook for pharma M&A continues to be strong, writes Michael Jewell.


Paul Brooks

Latest:

RAPS Statement - BREXIT delay

Regulatory Affairs Professionals Society's Executive Director, Paul Brooks, discusses the looming uncertainty about what will happen after the UK leaves the European Union as many important details remain unclear.


Jean-Francois Denault

Latest:

Measuring Product-Market-Fit

Jean-Francois Denault outlines a systemic approach to evaluating the commercial viability of a product.


Christian Rack

Latest:

Work Planning and Approaches to Overcome Bottlenecks – an analytical department in drug development

Common strategies to overcome bottlenecks and how fast they might lead to results are discussed.



Sudip Parikh

Latest:

Primed for Progress: FDA’s Pre-Cert Program for Digital Health Devices

Executives from DIA, Ranjini Prithviraj and Sudip Parikh discuss documents the FDA released that further detail the agency’s implementation plan for its Software Precertification Pilot Program.


Ranjini Prithviraj

Latest:

Primed for Progress: FDA’s Pre-Cert Program for Digital Health Devices

Executives from DIA, Ranjini Prithviraj and Sudip Parikh discuss documents the FDA released that further detail the agency’s implementation plan for its Software Precertification Pilot Program.


Angi Robinson

Latest:

Gene Therapy: Managing the Clinical Trial Minefields

Advice for developers in steering gene therapies from concept to trials to hopeful approval in what is an uniquely complex path.


Alyssa Palmer

Latest:

Operations: Gateway to Success in Cell and Gene Therapies

Life sciences therapies are moving away from a one-size-fits-all approach to a targeted approach using a patient's own genetic information and immune system to treat previously incurable diseases.


Shankar Suryanarayanan

Latest:

Operations: Gateway to Success in Cell and Gene Therapies

Life sciences therapies are moving away from a one-size-fits-all approach to a targeted approach using a patient's own genetic information and immune system to treat previously incurable diseases.


Prashant Yadav

Latest:

Operations: Gateway to Success in Cell and Gene Therapies

Life sciences therapies are moving away from a one-size-fits-all approach to a targeted approach using a patient's own genetic information and immune system to treat previously incurable diseases.


Devendra Mishra

Latest:

Operations: Gateway to Success in Cell and Gene Therapies

Life sciences therapies are moving away from a one-size-fits-all approach to a targeted approach using a patient's own genetic information and immune system to treat previously incurable diseases.


Jianan Huang

Latest:

A Formula for Rescuing Drug R&D

Jianan Huang discusses how the drug revenue formula is being used to guide R&D "rescue strategies".


Lisa Walkush

Latest:

Reinventing Pharma’s Talent Search

Thinning talent pools, combined with evolving industry trends and job-seeker motivations, are testing traditional pharma hiring methods, where targeting new skills and capabilities must become the new norm.


Jacinta Calverley

Latest:

Reinventing Pharma’s Talent Search

Thinning talent pools, combined with evolving industry trends and job-seeker motivations, are testing traditional pharma hiring methods, where targeting new skills and capabilities must become the new norm.


Cissy Young

Latest:

Hiring a Chief Diversity Officer

Nine ways pharma companies can maximize a CDO’s potential value and impact on driving innovation as a business mandate.


Sean Dineen

Latest:

Hiring a Chief Diversity Officer

Nine ways pharma companies can maximize a CDO’s potential value and impact on driving innovation as a business mandate.


Lital Aravot

Latest:

Mapping Out the Future of Cell and Gene Therapy

The cell and gene therapy space remains fertile territory for growth, exploration, and discovery. How applying a data-driven model may be the best way to approach this complex ecosystem and assess the innovations of tomorrow.

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