News

In an interview with Pharma Commerce Editor Nicholas Saraceno, Dan Gagnon, UPS Healthcare’s VP of Global Strategy & Acquisition Integration, discusses the development of frozen/cold biologics when it comes to the logistics space, along with how the companies themselves have changed over the years.

The climb is headlined by a 14.1% increase in total demand, according to the IATA.

Peter Ax provides insight as to industry’s lack of supply, along with how to mitigate these issues.

Gallagher’s 2024 US Physical & Emotional Wellbeing Report outlines ways to meeting evolving needs in the workforce.

The agreement focuses on augmenting the patient support experience, including from an adherence perspective.

The partnership—which features a $150 million investment—is also centered around vaccine development in the respiratory and immunology space.

A cohort study investigates whether or not the prevalence of these types of illnesses can vary among individuals who are COVID-positive versus negative.

The pre-approval pertains to a solid oral dose product that the CDMO will manufacture for a global pharmaceutical company.

Making connections between different datasets is essential to developing impactful medicines and driving more personalized patient care.

The parties will continue to create new candidate therapies for the treatment of a severe form of TUBB4A leukodystrophy.

A deep dive into why this therapy has demonstrated effectiveness in various areas, including for tumors.

The San Antonio facility will be taking this biomanufacturing initiative by the end of Q3 2024.

The deal exponentially grows the CDMO’s biopharma capabilities.

In a transaction valued at $250 million, the deal makes Grünenthal the new owner of Movantik, which treats OIC in adult patients with chronic non-cancer pain.

The latest news for pharma industry insiders.

Investigators evaluate differences in end-of-life care between Medicare beneficiaries in Medicare Advantage vs. traditional Medicare.

Analyzing the divergent paths undertaken by small biotech and large pharma companies in drug development.

FDA to review one-year results for Susvimo showing non-inferior visual acuity gains in diabetic macular edema and in the Diabetic Retinopathy Severity Scale for Diabetic Retinopathy.

In an interview with Pharma Commerce editor Nicholas Saraceno, Matthew Walsh, ixlayer’s general manager of biopharma, dives into efficiencies presented by at-home diagnostic tests.

In an interview with Pharma Commerce editor Nicholas Saraceno, Matthew Walsh, ixlayer’s general manager of biopharma, discusses findings of a new physician survey that the company conducted.

The agreement revolves around providing and maintaining supply chain transparency.

The financial commitment includes a pair of expansion plans occurring in the United States and Europe.

How teamwork among safety-net healthcare providers and pharma can make the difference.

The 50,000 square-foot facility has the ability to handle various batch sizes and dosage forms.

The clinical supply facility undergoes a $25 million expansion, welcoming 32,000 more square feet of temperature-controlled storage.

A study explores the cost-effectiveness of combining methotrexate with various drugs as a way to combat failed methotrexate monotherapy.

The construction of 100,000 square-foot facility will boost the site's filling capacity to 140 million units per year.

Why they are a game changer, and ways to a adapt to a new era of state privacy regulations.