Key industry trends and how the relationships between companies and CDMOs are evolving to better meet the challenges of a BANI world.
What pharma needs to do to keep up with the rise in value-based care.
With heightened government scrutiny on educational forums, biopharma manufacturers need a sound framework that demonstrates they are following best practices.
Andrew Hood and Cliodhna McDonough look at the key issues necessary to support business and the community in developing a long-term and sustainable response to the challenges highlighted by COVID-19.
Using market access data from day one of your drug development and commercialization journey puts your brand in the best position to succeed at launch.
Key traits needed by leaders looking to grow their organizations in the biosimilars market.
Increase in new treatments also brings increase in logistical challenges for pharma.
Delivering better patient outcomes hinges on innovation and adaptability.
Prioritizing deeper customer insights helps life sciences marketers understand how to engage their HCP audiences effectively with the right message.
Investments setting up sector for future success that could one day rival its US counterpart.
Faster launch planning leads to greater access.
Cybersecurity vulnerabilities embedded in AI and machine learning pose significant litigation risks as life sciences companies move to digital technologies.
There is considerable variation in the regulatory approach to medical cannabis between European countries. Yet, despite the complexity, there are clear routes to market, reports Peter Kohut.
The current vaccine pipeline brings promise of significant global health advancements—yet development gaps remain, and the future delivery challenges must be considered.
The new Goochland County facility will serve as Lilly’s first fully integrated API and drug product site, focusing on antibody-drug conjugates, while creating thousands of jobs and strengthening domestic supply chains.
The key steps for pharma in pivoting from proof-of-concept experimenting to enterprise-scale value.
Pathways to success for this key component of Europe’s new HTA regulation, where thinking beyond the purely technical will be critical.
Three ways artificial intelligence can drive the necessary engagement between patients and HCPs.
Outlining the implications of this c-suite trend for pharma.
Addressing the increased use of technology in safety compliance processes and greater patient involvement.
While patient support providers play an important role in keeping patients on therapy, biopharma companies have a great opportunity to push analytical sophistication beyond what many of these providers currently offer.
Forging effective partnerships with local companies is particularly important when entering Brazil’s pharma market. Sameer Kolhe reports.
Will the FDA ultimately step in and mandate a credible effort to eradicate the mindset that long-term adherence is not achievable?