Through embracing connected and tech-enabled services and devices, new avenues and opportunities exist for greater clinical trial flexibility in drug research.
Rafael Teixeira on building an end-to-end cold chain strategy to support global storage and distribution efforts.
Better technology is redefining pharmacovigilance as it expands beyond its traditional compliance focus to become a key business differentiator.
The future of CAR T-cell therapies will continue to improve as they expand to other patients in need.
Three key components to scaling quickly—while maintaining purpose.
Pharma and life science companies can reduce time to market by optimizing regulatory content management and submission processes.
Identifying the inflators and deflators, and the role all stakeholders play.
The massive shift to remote work has seen pharma companies increasingly targeted by malicious actors seeking out weaker points across the business ecosystem. But with the right mix of technology and mindset, organizations can prepare against threats in the future.
The future of CAR T-cell therapies will continue to improve as they expand to other patients in need.
In a time of global pandemic, traditional vaccine procurement schemes are not fit for purpose and need to adapt to allow both governments and manufacturers the ability to manage a greater level of risk associated with rapid vaccine development and deployment.
Silicon Valley Bank has collapsed, leaving many biotechnology companies unsure of the future.
The importance of life sciences companies focused on rare diseases to take early steps to bridge connections with patients, caregivers, and healthcare providers.
Although life science organizations are not immune to the benefits of artificial intelligence, it’s important to integrate it with caution because there is no “one-size fits all” approach.
Here are three mindsets for pharma companies to adopt now to reap the rewards of early action in the metaverse.
There are several strategies life sciences companies can use to benefit from biosimilars.
The recent FDA approval of Biogen’s controversial drug aducanumab is the first drug approved for Alzheimer’s disease in nearly 20 years, and highlights the urgent need for new disease modifying approaches in drug development in this indication.
The COVID-19 pandemic has shifted the adoption of digital platforms in pharma and has made the industry reconsider which technologies can improve global health moving forward.
Failed efforts do not overshadow field’s progress, resolve.
These factors provide investors with enough information to identify promising investment opportunities.
Explicitly tying strategic planning to resource allocation boosts bottom-line productivity for pharma.
Commercializing an orphan drug can be challenging, however, using a framework and a checklist that incorporates the right elements can prove beneficial.
Mark Davies and Paul Riley outline their blueprint for exploring how healthcare companies can leverage real-world evidence to access and engage customers more effectively.
In an era where business-critical information is exchanged instantly, unsecured communication channels are a significant risk.
With small biotechs facing similar expectations as large pharma in drug safety and pharmacovigilance, despite less resources, identifying the key differences between US and EU requirements can help these companies craft a practical path to multi-region compliance.