Authors


Jasmine Mui

Latest:

How Medical Affairs Can Contribute to Successful Drug Launch

Faster launch planning leads to greater access.


Mark McLaughlin

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.


Cecile Riboud

Latest:

10 Practical Regulatory Questions to Ask During a Marketing Authorization Transfer Process

With large M&A deals comes a complex Market Authorization Transfer (MAT) process, during which regulatory teams must weigh several operational aspects while creating a roadmap that takes them into account. Cecile Riboud outlines some key questions that are necessary for planning and executing a successful MAT process.


Catherine Owen

Latest:

Embracing the Future: Meeting Doctors and Patients Where They Are Now

Pharma companies must embrace the future to advance commercialization.


Matt Norton

Latest:

Creating a Digital Solution Patients and HCPs Will Use

Developing a digital health solution that patients and HCPs will use requires creating technology that addresses unmet needs, integrates with clinical care pathways, and has strong user safeguards, writes Matt Norton.


Seth Lederman, MD

Latest:

Why Are We Surrendering to COVID?

Industry must continue research and development to combat the pandemic.


Harris Kaplan

Latest:

Marketers: Physicians are People First

Understanding the changes in day-to-day life for physicians during COVID and how life science executives can address them.


Flatiron

Latest:

Unlocking Oncology Insights - Innovations in Evidence Generation With RWE Solutions

The rapid evolvement of precision oncology requires real-world data generated at a scale that unlocks insights that can not be provided from clinical trial evidence. Machine learning and large language models can be used to quickly identify information, supporting custom integrated real-world evidence solutions to make informed decisions.


Prabhjot Singh

Latest:

Omnichannel Marketing Challenges for European Life Sciences Companies: A Data Science Perspective

As EU brand leaders build their omnichannel customer engagement strategies, they need to address challenges in the European environment with a well-thought-out deployment plan.



Evan Loh, M.D.

Latest:

Don’t Waste A Crisis: How Paratek is Navigating the Business Implications of the COVID-19 Pandemic

A look at how pharmaceutical company, Paratek is navigating the launch of a new antibiotic during the COVID-19 pandemic.


Matthew Arnold

Latest:

Biotech’s Survival Story: Companies Bear Down for Lean Years

While large pharma investment in biotechs is down—as pharmas become more strategic in their selections—it is scarcely out, with the partnership dynamic between the two sides remaining strong.


ON24

Latest:

Redefine the Digital Experience for Life Science Innovation

Tuesday, June 29, 2021 at 2pm EDT | 1pm CDT | 11am PDT


Divya Yerraguntla

Latest:

How Should Biotechs Strategize for 2025

Strategic imperatives for biotech firms in light of the latest market dynamics and investor behaviors.


Tong Wang and Justinian Liu

Latest:

China 2021: The NRDL Readout

China‘s 2021 National Reimbursement Drug List (NRDL) results are finally out, and this year features another major expansion of the NRDL formulary, with ongoing emphasis on innovations and some much anticipated breakthroughs in rare disease drug inclusions.


Asaf Evenhaim

Latest:

It’s Time for a Fresh Approach to Patient Data in Rare Disease

Current practices leave much to be desired with increasing commercial needs.


Anne Ollivier

Latest:

New Product Planning: The Function's Evolution in Pharma

With an organization's future commercial success under its remit, the NPP function has rapidly progressed to a prominent role in the biopharma industry—but evidence-generation strategies must evolve with an eye toward emerging trends and technologies.


Ed Kloskowski

Latest:

The C-Suite’s Frontline Workers in Digital Change

How the CIO role has transformed and strengthened against the backdrop of COVID-19.


Simon Johns

Latest:

The Agile Future of Medical Information: Meeting 21st-Century Demands for Healthcare

COVID-19 pandemic has accelerated raised expectations for medical information professionals.


Adam Andersen

Latest:

At the Heart of Pharma: ESG has Arrived as a Central Strategy

Pharma supply chains are no longer hidden beyond the reach of ESG agendas, making it important for companies to accelerate adoption of new manufacturing processes and environmental technology.



Anton Yazovskiy

Latest:

Is Your Demand Side Platform (DSP) Ready for the Cookieless Future?

A cookieless future is on the horizon, so marketers across all industries are being forced to rethink their strategies and plan for the future. What does that entail?


Wesam Badran

Latest:

Realizing the NHS’s Digital Potential

Wesam Badran looks at how the UK NHS can collaborate with pharma and med-tech partners to encourage digital innovation.


Acceleration Point

Latest:

5 Challenges of Increasing Online Scientific Discussion

Wednesday November 9, 2022, 11am EDT | 8am PDT Discover insights and find ways to engage in the 24/7 world of online digital scientific exchange. Learn to listen to digital opinion leaders and find opportunities to engage.


Jacob Graham

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.


Currien MacDonald, MD, CIP

Latest:

Cleared and Graded: Modernizing the 510(k) Pathway

Due to increasing complexity of modern technology, FDA should consider updating its 510(k) process.


Dr. Judith M. Sills, PharmD

Latest:

Navigating PV Divergence: Compliance Tips for New Entrants

With small biotechs facing similar expectations as large pharma in drug safety and pharmacovigilance, despite less resources, identifying the key differences between US and EU requirements can help these companies craft a practical path to multi-region compliance.


Emily Lockey

Latest:

COVID-19: Is the Vaccine Race Over?

Cliodhna McDonough and Emily Lockey give a UK perspective on the potential pros and cons of the three leading candidates in the COVID-19 vaccine race.


Theresa Vuskovich

Latest:

Addressing the Knowledge Gap in Biologics & Biosimilars: Is a Board Certified Biologics and Biosimilars Program the Answer?

Life sciences professionals will need to keep up with market demand for biologics and biosimilars.


Ashwin Singhania

Latest:

Commercial Models for the Changing Life Sciences Market

Life sciences companies have an opportunity to craft a sales approach that resonates with clients, protects against future disruptions and stands out from the competition.