Recent events can provide digital therapeutics companies with clear lessons for the future.
Despite the rapid innovation of machine learning, correct protocols to ensure compliance and trustworthiness must be considered.
How to cultivate trust & connections in life sciences in a time of AI bias.
Biopharma has a responsibility to meet patients where they are.
To successfully commercialize orphan drugs, companies need to set aside general medicine strategies and adopt a more granular approach to identifying and capitalizing on commercial opportunities.
Commercial Health Insurance may bring more opportunities for market access in China.
How pharmaceutical companies can utilize AI at key stages of the treatment journey to enhance patient-centric engagement by increasing empathy and humanity in patient interactions.
With opportunity and risk lurking in equal measure, today’s key considerations for biopharma startups when building their leadership teams and product go-to-market strategies are outlined.
Presenting a structured, decision-making approach for executive management to make sound strategic decisions for drug development and life cycle management.
Improvements in R&D, manufacturing, and data sharing will extend platform’s reach.
Pharmaceutical Executive, in collaboration with Biofourmis, organized a roundtable of experts from various groups to discuss how digital medicine and pharmaceuticals are changing the trajectory of what drug development and clinical care look like together, with an emphasis on partnerships within digital health.
A modern healthcare ecosystem involves various stakeholders and many forms of complex data. Collaborations and a range of advanced approaches are essential to providing more uniform and complete healthcare to patients.
Genpact’s latest report, Life Sciences and Healthcare in the Age of Instinct, explores three major trends shaping the future of healthcare.
Education and knowledge transfer must be prioritized for industry to see sizable improvement in medical affairs.
The Medicare Part D cap won’t solve need for financial assistance.
Pharma companies and RPM manufacturers must work together to find solutions to make DCT more commonly available.
A fresh look at how industry benchmarks can help fortify new drug launches to overcome today’s new market-entry barriers and higher expectations.
GenAI is on the precipice of breaking new ground in regulatory intelligence; making strategists more efficient by alleviating challenges, streamlining regulatory research and submission processes.
at some point, we won’t be seeing wall-to-wall COVID coverage anymore, but stories about the fallout. How can pharmaceutical brands prepare for what’s next?
Top industry experts weigh in on what the new year holds for the pharma industry.
New regulations may require regulators to explore new payment options.
Precision & Specialty Medicines are driving changes in the pharma development industry. We explore the changes these paradigms are having on the clinical trial space.
Significant challenges still lie ahead, but several specialists and a plethora of new technologies are well positioned to gather and analyze the evidence needed for diagnosing and treating rare diseases, writes Catherine Tak Piech.
Exploring the importance of analytics as a means of staying competitive in the commercial pharmaceutical market.
MIDD can pave new road for drug development.
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.