Collaborative efforts among researchers, clinicians, and industry are essential to unlock the full potential of digital health in transforming the lives of people with Parkinson's disease.
A look into the traits that hiring managers of pharma companies should be searching for when hiring for a leadership role.
Virtual audits proving to be beneficial post-COVID despite continuing challenges.
While challenges remain, AI is accelerating the process by enabling researchers to identify and design new drug candidates more quickly and efficiently with applications in target discovery, structure prediction, and drug optimization.
CMS’ draft guidance on real-world data study protocols marks a significant move toward transparency and rigor in Medicare coverage decisions.
In many plants, the full expression of therapeutic value only emerges when their components are allowed to work in concert.
Bridging the gap in data utilization and knowledge/learning management is crucial for successful drug development.
How to maximize market-entry performance for new pharma products in an increasingly competitive launch environment.
Pharma companies are now under increasing pressure, and increasingly willing, to offer a patient-centric approach. But with this increasing demand comes confusion about what patient-centered research actually is.
Patient support programs (PSPs) have an opportunity for growth and innovation.
Amid the shifting focus from primary care to specialty care, using data-driven tactics can create tailored campaigns and meaningful relationships with nurse practitioners and physician assistants.
Planning for a post-recession scenario is essential, ensuring companies are prepared to scale up when funding permits.
Delivering value with enterprise program management.
Patient centricity and access highlight keys to success for new development.
Artificial Intelligence (AI) fueled by real-world healthcare data has yet to be fully leveraged by biopharmaceutical companies but is poised to revolutionize their business strategies.
Ecolab is looking to the future with new opportunities to partner with Pharma for critical solutions to support drug development and manufacturing.
How PREP Act protections will apply to potential COVID-19 vaccine-related claims.
Addressing the challenges faced by Global Medical Affairs teams and how they can find balance to create maximum value for their organizations.
Amid lingering questions and uncertainty, a look at ways pharma companies can prioritize incorporating the Inflation Reduction Act into their strategic planning process—and do it now.
A look at China's emergence as a hub for novel treatment pursuits—and ways international investors can best capitalize on the favorable research trajectory.
The Medicare Part D cap won’t solve need for financial assistance.
Opportunity remains despite regulatory and access obstacles.
Evolving preferences of HCPs during the pandemic have put an emphasis on learning new skillsets for pharma reps.
The introduction of alternative payment models and specialty pharmacy benefit management (SPBM) is poised to usher in a new era of affordability for expensive gene therapies.
Whether your company already has a data-driven compliance program in place or is contemplating building one, Michael O'Connor and Isha Arora outline four things the DOJ is now focused on that your compliance team needs to know.
When deciding on the right commercialization model, organizations must consider multiple factors, including the asset or platform they possess, the launch timing, the funding required, and staffing expertise.