Biopharma companies can foster patient-centered innovation by focusing on unmet needs along each stage of the patient journey while collaborating with key stakeholders directly or indirectly responsible for disease management.
Key Challenges for Manufacturers and How MilliporeSigma is Leading Industry-Wide Change
Addressing sources of tension on differentiating types of data.
A discussion with medical leaders on the present and future state of this vital biopharmaceutical function.
Wearable sensors and remote monitoring technology can help HCPs monitor and manage COPD more effectively.
Pharm Exec’s 19th annual report on the trends of the day in drug development examines the surging investment in new treatments and advances for so-called “first-world” conditions, capturing the landscape of five expanding therapeutic areas: weight loss, osteoarthritis, Alzheimer’s disease, COPD, and psychedelics.
Understanding of recent legal developments can help companies avoid infringement.
Ferdi Steinmann looks at pharma's current relationship with AI and how it is set to evolve.
If the life sciences sector can support healthcare professionals to gain confidence in substituting original treatments with new biosimilars, prices will reduce and patient outcomes will be enhanced.
***Live: Thursday, February 25, 2021 at 11am EST | 8am PST | 4pm GMT | 5pm CET*** As strategic planning among manufacturers and logistics partners commences, this webinar will serve as a platform to discuss service offerings and explore the most effective possible solutions. *** On demand until Feb. 25, 2022***
Mitigating the risks of development, authorization, and marketing for new therapies following "new normal" created by COVID-related violations.
Looking to the past reminds industry of great strides taken in clinical research for patients.
Matthew Howes, President at Greater Than One, discusses what to expect in the next twelve months in healthcare marketing.
A look at the rise of prior authorization certified specialists (PACS)—and their value in improving patient access and outcomes.
A look at how pharmaceutical company, Paratek is navigating the launch of a new antibiotic during the COVID-19 pandemic.
Including patient and family feedback in our discussions will help shape our understanding of their perception of provided care and services and how we operate as a whole.
Cybersecurity vulnerabilities embedded in AI and machine learning pose significant litigation risks as life sciences companies move to digital technologies.
Historically, Medical Affairs teams have relied on reporting only empirical evidence such as efficacy and tolerability profiles to influence uptake of a new drug or therapy. Here, Ben Routley and Mark Pringle explore the scope for applying behavioral science techniques to improve the impact of client communications.
U.S. patent law will have to adapt to the use of AI in the life sciences industry.
IT Leaders in Life Sciences discuss the consolidation of the learning tech environment to help shift the training effectiveness conversation from anecdotal evidence to data-driven understanding.
Pavel Klymenko, Head of Omnichannel at Viseven, compares three top approaches to pharma communication and elucidates which are here to stay.
There are clear pathways that biopharma companies can take to sustain growth and remain competitive.
Key steps in relationship-building beyond just treatment options.
Best practices for defending against lawsuits based on pharmaceutical labeling, including avenues for early resolution of the case and, as necessary, strategies for developing the best evidence for defense.
Several months into the COVID-19 pandemic, this article takes a look back at how the launches of new oncology therapies have been impacted.
Webinar Date/Time: Wed, Nov 1, 2023 11:00 AM EDT