The importance of KOIs in tapping into today’s market mindset.
The importance of KOIs in tapping into today’s market mindset.
Yesterday, the Supreme Court heard arguments on the matter of pay-for-delay settlements between patent holders and generic firms.
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.
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.
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?
Patient support program providers should incorporate new technologies for more effective processes, but this should be matched with empathy, human connectivity and personalized clinical interventions, writes Tommy Bramley.
Steve Gens and Remco Munnik offer five best-practice tips for achieving a definitive, trusted regulatory and product information asset base capable of supporting intelligent innovation.
The impacts of disruptive curative therapies and advances in the future of health will be profound. To be best positioned for success, healthcare systems under continuous cost pressure must address three key areas, writes Thomas Unger.
Dr. Steven Fox, CEO of Akelos Inc., discusses the challenges of developing new non-opioid medical products as the need intensifies as the crisis worsens.
Reoccurring disappointment in development portfolios-why it happens and how to mitigate it.
The Identification of Medicinal Products (IDMP) software industry has talked up the broader potential of data-driven processes. Pharma companies and their software providers have an important role to play in realizing these processes. Frits Stulp discusses the foundations that need to be laid for lasting transformation of pharma information access in the real world.
Biopharma companies hungry for digital talent must evaluate their real estate portfolio and workplace strategies to access new talent pools, says Joanne Henderson.