Podcast: Rare Disease Day: FDA guidance allowing advancement
It’s been a busy year for rare disease developers, with the US Food and Drug Administration (FDA) releasing several new…
It’s been a busy year for rare disease developers, with the US Food and Drug Administration (FDA) releasing several new…
Developers in rare disease emphasise cashflow and R&D expansion as evidence of their transition from emerging biotechs to established companies…
Bristol Myers Squibb (BMS) is confident pivotal readouts from its core pipeline will drive profits towards 2030 despite looming patent…
The US Food and Drug Administration (FDA) has announced increased flexibility for cell and gene therapy (CGT) manufacturers, loosening quality…
Patient burden should join standard operational metrics like cost, timelines, and regulatory compliance to ensure long-term clinical trial success, argues…
Closer relationships with clinical trial partners are key to ensuring long-term trial success with German pharma giant Bayer, says the…
Artificial intelligence (AI) is expected to not only supplement clinical trials, but redefine the sector, while the industry braces for…
Regulatory overhaul, international trade tariffs, and the burgeoning disruption imposed by artificial intelligence (AI) are moving the clinical trials industry…
Tariffs imposed by President Trump on US pharma imports have left experts charting a new course for the nation’s clinical…
Against the backdrop of geopolitical tensions and economic measures such as tariffs, which are influencing supply chains across numerous industries,…