Biopharma must step up amidst growing oncology market.
How companies are leveraging Real Word Evidence to evaluate therapies under real world conditions in a broader population at a lower cost than using Randomized Clinical Trials.
When patients struggle to see a positive path forward, modeling a constructive journey can give them the confidence they need.
Understanding of recent legal developments can help companies avoid infringement.
Their integration across enterprise remains pivotal driver for success.
Country is poised to offer growth-channel opportunities for global pharma companies ready to scale access, innovation, and profitability.
In adjusting to the long-term aftershocks from the coronavirus pandemic, pharma companies will need to focus on change in three core areas.
The era of big pharma as product-first companies must end, as services become the larger priority.
In an unpredictable world, international life sciences collaborations can lead to misunderstandings and enforcement challenges, making an effective dispute resolution mechanism an essential risk management tool.
Donald Macarthur and Dr. Meriem Bouslouk-Marx discuss post-approval findings of national committees in Europe charged with deciding the best strategy to use a new COVID-19 vaccine in their populations.
In the rapidly changing fields of medicine, such as hematology/oncology and specifically with respect to the management of patients with chronic lymphocytic leukemia (CLL), education is a key component of keeping clinicians current on changes to treatment paradigms.
The growing complexity of supply chains necessitates the adoption of collaborative planning processes and capabilities such as S&OP and S&OE.
Companies must determine the right ways to utilize AI.
Insights and examples of how collaborative efforts can lead to the development of innovative therapies that target unmet patient needs.
A proactive and tailored compliance department—with the nimbleness to adapt strategies on the fly—is a critical shield for life sciences companies during government investigations.
The stakes have never been higher.
Providing ultimate value to stakeholders remains key in new style of development.
U.S. patent law will have to adapt to the use of AI in the life sciences industry.
As regulatory reform continues to evolve in the US and Europe, the role of regulatory affairs is poised to help shape the more personalized treatment landscape on the horizon.
NJ can regain leadership in pharma by offering modern lab spaces for biotech and other lab-based growth companies.
Analytics capabilities are no longer a nice-to-have, but a necessity to build and maintain a successful business and competitive edge.
Amy West, Head of US Digital Health & Innovation Strategy at Novo Nordisk, shares her insights on fostering collaboration, embracing change, and her compelling vision to revolutionize digital transformation and innovation in the field of healthcare.
Stay-at-home orders during the pandemic forced a shift in patient preferences—and the pharma industry has responded.
Addressing the challenges created by virtual meetings with HCPs, what we have learned about virtual meetings so far, and a look into the future.
Life sciences professionals will need to keep up with market demand for biologics and biosimilars.
How a large, global biopharma company is leveraging a data-linking strategy to power insight-generation tools and techniques—and supporting customers through their journey with dynamic personalization and modular content.
Webinar Date/Time: Thu, Oct 9, 2025 11:00 AM EDT