Advancements in periodontal disease could make way for expansions in the dental space and other medical fields.
While hurdles remain, home healthcare could deliver better patient-centered cancer care—providing improved outcomes, enhanced quality of life, and reduced strain on resources.
In today’s pharmaceutical market access landscape, payers are not the sole decision-makers in utilization management development.
Devesh Verma and Rebecca Lorenzo outline some the challenges and potential solutions to building a patient-centric culture
Lise Stevens explores what difference the ISO IDMP (Identification of Medicinal Products) data standards would have made in a COVID-19 context — in applications ranging from pharmacovigilance adverse event reporting and electronic prescribing to falsified medicines control.
Changes necessitated by COVID will drive unprecedented transformation of industry.
The 2022 National Reimbursement Drug List will see more pressures for new inclusions on the one hand, and more certainties for renewals on the other. At the same time, the process is becoming more interactive and transparent.
It’s time for pharma brands to recognize the potential of TikTok as a promotional platform and develop a strategy to not only stand out but make an impact.
Soaring healthcare costs show little sign of slowing in 2024, with concerns growing about the affordability of medications and medical services.
It's time to apply the same COVID-19 urgency to other devastating diseases, such as Alzheimer’s, write Andrea Pfeifer and William Mobley.
The world’s largest cancer research meeting, the American Society of Clinical Oncology (ASCO) Annual Meeting, recently convened in person in Chicago after two years of being held virtually. Sara Baker and Kristine Austria Fan of Marina Maher Communications provide their takeaways from the meeting.
NJ can regain leadership in pharma by offering modern lab spaces for biotech and other lab-based growth companies.
What the c-suite should consider in today’s marketplace.
How drugmakers can better harness real-world evidence to drive their clinical and commercial objectives, while also providing greater clarity for healthcare providers and improved access to therapy for the patients they serve.
Why enabling a shared culture of quality across an organization is key to maintaining pharma’s recent pace of innovation wins—while inspiring new levels of confidence.
Importing drugs from Canada may increase the risk of US citizens being exposed to unsafe medicines.
The importance of pre-approval information exchange (PIE) with payers and other strategic considerations to help navigate today’s market access challenges and regulatory requirements in bringing promising cell and gene therapies to the market.
Recent growth in pharma makes Ireland an ideal candidate for expansion opportunities.
Despite disruption from the COVID-19 pandemic still in full swing, life sciences innovation activity remained undeterred, a recent report from the IQVIA Institute for Human Data Science finds—outlining the key factors driving record-breaking growth.
Understanding of recent legal developments can help companies avoid infringement.
Oncology drug developers must start asking questions in preparation of FDA’s dose optimization initiative.
The benefits of diversity in the workplace are far-reaching — not just for employees, but for a company’s overall health.
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.