Pharm Exec introduces new monthly columns.
When we redesigned Pharmaceutical Executive in May 2020, we included four new monthly columns: leadership, technology, finance, and strategy. These were topics we felt were top-of-mind for our readers and we wanted to dig deeper into the issues and trends affecting these areas. Over the past two years, we’ve added marketing and managed markets columns.
As we continue to evolve and serve the biopharma community, we’ve decided to make some additional changes to our coverage. We’re folding our existing columns into quarterly rotations with two new, exciting themes. These new columns will focus on the important, timely topics of diversity, equity, and inclusion (DE&I), and environmental, social, and governance (ESG).
Beginning with this issue, we will rotate DE&I, ESG, and leadership columns in one group. Another quarterly group will consist of managed markets, technology, and marketing. We felt that these topics organically fell into these groupings, as many of their themes often overlap.
Our new coverage kicks off this month with our new DE&I column, authored by Denice Torres. Torres is a senior healthcare executive and board member of Resilience, Surface Oncology, 2seventy bio, Glaukos, and Karuna Therapeutics. She is the founder of The Mentoring Place, a free career mentoring program for women, and CEO of The Ignited Company, a change management and DE&I firm. She also has a podcast, “Flip the Tortilla: Lessons for the Underdog at Heart,” on all major platforms. This month, Torres talks about how hybrid workplace decisions can impact DE&I dynamics.
Next month, we will debut our ESG column, contributed by Geralyn Ritter. Ritter is head of external affairs and ESG at Organon. In this role, she focuses on guiding and shaping how the company interacts with key stakeholders and the environment. We’re excited to have her industry input on this important topic.
Separately, our Global Report has been renamed Europe Report, and we’ve added a quarterly Asia-Pacific (APAC) column—debuting this issue—to provide a deeper look into each of these key regions. Our APAC columnist, Bruce Liu, is a partner at Simon-Kucher & Partners and leads the company’s life sciences division in greater China. He has more than 20 years of experience in the APAC healthcare industry across diverse therapeutic areas. In this month’s installment, he discusses China’s growing cell and gene therapies market.
Finally, Barbara Ryan’s insightful finance articles will remain a monthly theme. We value her expert analysis on topics such as the long-term effects of the biotech bear market, mentioned this issue. Longtime contributor Jill Wechsler’s Washington Report, covering important and timely policy news, will also remain monthly.
To recap our revamped coverage, you can expect two rotations: DE&I/ESG/leadership and managed markets/technology/marketing. Asia-Pacific will run quarterly. Europe, finance, and Washington Report will remain monthly features.
As our dynamic industry changes, we will continue to evaluate our coverage to include areas of emerging interest, delivering all the pertinent information you need to be successful.
Elaine Quilici is Pharm Exec’s Editor-in-Chief. She can be reached at equilici@mjhlifesciences.com
Asembia 2025: Therapy Advancements Highlight Growing Cost and Access Concerns
April 30th 2025Fran Gregory, VP, emerging therapies, Cardinal Health, discusses the evolving cell and gene therapy landscape, highlighting pipeline growth, cost challenges, and emerging therapeutic areas beyond oncology and hematology.
Addressing Disparities in Psoriasis Trials: Takeda's Strategies for Inclusivity in Clinical Research
April 14th 2025LaShell Robinson, Head of Global Feasibility and Trial Equity at Takeda, speaks about the company's strategies to engage patients in underrepresented populations in its phase III psoriasis trials.
FDA Approves Nipocalimab for the Treatment of Generalized Myasthenia Gravis
April 30th 2025Approval is based on results from the pivotal Vivacity-MG3 trial in which IMAAVY (nipocalimab-aahu) demonstrated superior disease control throughout 24 weeks when compared to placebo plus standard of care.
Beyond the Prescription: Pharma's Role in Digital Health Conversations
April 1st 2025Join us for an insightful conversation with Jennifer Harakal, Head of Regulatory Affairs at Canopy Life Sciences, as we unpack the evolving intersection of social media and healthcare decisions. Discover how pharmaceutical companies can navigate regulatory challenges while meaningfully engaging with consumers in digital spaces. Jennifer shares expert strategies for responsible marketing, working with influencers, and creating educational content that bridges the gap between patients and healthcare providers. A must-listen for pharma marketers looking to build trust and compliance in today's social media landscape.
FDA Approves AbbVie’s Rinvoq as First Oral JAK Inhibitor for Giant Cell Arteritis
April 30th 2025AbbVie secures FDA approval for Rinvoq as the first oral Janus kinase inhibitor indicated for giant cell arteritis, expanding its immunology portfolio and signaling strategic growth opportunities in underserved autoimmune markets.