While culture may "eat" strategy, shared understanding creates both culture and strategy, write Steve Figman and Sean Robertson.
How pharma companies can bolster their quality management programs to meet FDA’s evolving compliance requirements.
Global content management needs are mounting among life sciences organizations, as they expand their market coverage and grapple with multiplying regulatory workloads. Monica Vytiskova asks if can intelligent automation offer a solution.
If telehealth is here to stay, how is the industry adjusting?
The importance of KOIs in tapping into today’s market mindset.
The importance of KOIs in tapping into today’s market mindset.
At last week’s 4th annual Prix Galien Forum hosted by the Alexandria Center in New York, industry leaders gathered to discuss trends and developments that shape the intersection between science and policy.
A 2019 study reveals further marginal decline in the pharma industry's reputation. Sven Klingemann suggests some "recovery solutions".
Coexisting with the DSCSA may hinder new legislative efforts.
How to navigate the production and reimbursement intricacies of bringing regenerative medicines from bench to bedside.
How to navigate the production and reimbursement intricacies of bringing regenerative medicines from bench to bedside.
Four takeaway messages from the Zolgensma pricing storm
Outlining the critical steps for companies in controlling market exclusivity for their gene therapies.
Outlining the critical steps for companies in controlling market exclusivity for their gene therapies.
Outcomes-based contracts seem to have the potential to make drugs more affordable, but not without mutually-beneficial, data-driven arrangements.
The key steps to evading automation-fueled data crises.
Do’s and Dont’s while facing the increased war for talent.
Clive Glover and Mark Szczypka discuss the complexities of scaling up the manufacturing of gene therapies and gene-modified cell therapies to industrial levels.
Every healthcare company should be striving to identify better ways to ensure patients and consumers inspire every decision they make, writes Joanne Waldstreicher.
The US could theoretically treat every single American living with HIV without spending an extra dollar on drugs. And President Trump can broker a deal to do it, write Anil Soni and Ya’ir Aizenman.
Aiden Flynn discusses mining real-world data pools to transform drug development.
Ben Jacoby assesses the scope for disruption of the significant changes in medical device transparency and traceability requirements, and advises on a practical response.
The latest trends in patent litigation has led to a more harmonized patent system, which can benefit pharmaceutical companies that invest in patents.
A key question for an organization post-M&A is: “What organizational capabilities support global guidance and leadership, and which of them require these at the 'local' level?” Scott Hull discusses potential solutions.
Stephen Rivera, vice president, global technical accounting advisory services and policy, Johnson & Johnson, capitalizes on his lively personality—and a courageous career journey—to bring people together to shape the future of biopharma.
Is Congress harming pharmaceutical research by limiting enforcement of improvement patents?
Is Congress harming pharmaceutical research by limiting enforcement of improvement patents?