Delivers up-to-date industry news on topics like drug approvals, product recalls, company expansions and acquisitions, market trends for all OSD forms, as well as excipients, packaging and supply chain issues. Monitors market trends in specific drug categories as well as in supplements/nutraceuticals. Provides updates on clinical trials. Includes alerts about new or upcoming regulatory issues.
As a result, the company is currently restructuring to reduce its annual direct R&D spend by 60%.
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This past Friday, HHS placed Tidmarsh on administrative leave; two days later, he resigned.
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Lilly’s new $3 billion manufacturing plant in the Netherlands will produce oral medications, including its GLP-1 pill.
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Pfizer has called Novo’s unsolicited buyout bid “an illegal attempt by a company with a dominant market position to suppress competition.”
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Obesity med giant Novo Nordisk has submitted an unsolicited $9 billion proposal to acquire Metsera, outbidding Pfizer.
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After an initial delay, the Bayer's dual neurokinin targeted therapy, Lynkuet, has received FDA approval.
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BridgeBio reported positive topline results from a phase 3 pivotal study of its small molecule oral therapy in individuals living with limb-girdle muscular dystrophy type 2I/R9.
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Jascayd, an oral treatment for idiopathic pulmonary fibrosis, has received approval in China.
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If approved, the drug will be the first oral bone-building therapy for postmenopausal women with osteoporosis.
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The 400,000-square-foot facility will be located at Merck’s site in Elkton, Virginia, where the company has had a presence for almost 85 years.
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In a phased investment, ACG will construct and then increase capacity of its facility in Atlanta, Georgia.
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Fabhalta has hit its phase 3 goals for treating the progressive autoimmune kidney disease, putting it on a path to traditional FDA approval.
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VDPHL01 is the potential first and only extended-release oral minoxidil for women and men with pattern hair loss.
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The transaction will establish a standalone orthopedics business, operating as DePuy Synthes, within the next 18 to 24 months.
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The Delhi High Court has cleared Natco Pharma to launch its generic version of Roche’s spinal muscular atrophy drug.
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