Value-based price for access (VBPA) may increase access of specialty drugs for patients.
As the overall industry pipeline of allogeneic T-cell therapies expands, the onus on manufacturers and their partners to adeptly manage the complex cryogenic logistics process intensifies.
Adoption of digital by biopharma reps has added an element of flexibility to their engagement strategies, resulting in better communications with HCPs.
Omnichannel marketing bridges the gap from marketing operations to sales excellence. A well-planned, omnichannel marketing strategy allows pharma companies to reach the right people, at the right time, with the right message. Omnichannel marketing provides a holistic view of the customer to improve stakeholder experience across all touchpoints.
Life sciences professionals will need to keep up with market demand for biologics and biosimilars.
A robust market access strategy ensures that pharmaceutical products, including those with limited distribution, reach patients and are covered by diverse healthcare systems.
How pharmaceutical leaders at established companies can still disrupt the status quo and change the game.
Dr. Manuel Hermosilla shares his thoughts on how the pharmaceutical industry reacts to challenges that arise during trials, specifically during the search for an effective COVID-19 vaccine.
Findings from hundreds of interviews of exceptional pharma leaders around the world.
Harnessing the power of curiosity to position your next big idea
In the race to bolster pipelines and drive growth, biopharma manufacturers are reexamining traditional practices and reimagining market research protocols.
How can pharmaceutical companies successfully apply advanced analytics? Pricing experts from Simon-Kucher & Partners identify the hurdles and winning approaches.
The 2021 National Reimbursement Drug List (NRDL) process has been unfolding in China since June this year, with several key themes emerging. Building on Simon-Kucher’s experience with the NRDL, the authors make three recommendations on negotiation strategies going into the process.
A survey of 18 biopharmas, measuring their scope and implementation across key health equity dimensions and activities, uncovers useful context as companies seek better alignment of these goals with overall strategy.
The high-stakes nature of cancer care, coupled with rapid scientific advancements and increasing payer and regulatory pressures, demands a specialized approach beyond traditional market access strategies.
Value-based price for access (VBPA) may increase access of specialty drugs for patients.
As skepticism surrounding AI fades, pharma industry execs are ready to embrace the technology.
In this article, Eli Lilly & Co. examines risk management in the context of partnerships with other companies.
Automated risk management and improved regulatory compliance among opportunities offered by case collection.
HEOR scientists in the pharma industry must balance methodologic rigor with commercial expectations and timelines.
The redirection of healthcare and life sciences resources to COVID-19 has taken focus from other areas of need, including antimicrobial resistance.
Pharmaceutical companies are facing new guidelines, laws, and regulations requiring a reconsideration of how to prioritize, develop, commercialize, and ultimately, secure access to medicines.
Employees must be able to retain information and remain engaged to keep pace with highly regulated industry.
Opportunity remains despite regulatory and access obstacles.
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.
The emergence of organized customers demands investment in advanced solutions and next-generation key account management.