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August 02, 2022
Novasep-PharmaZell will increase API production capacity at its Mourenx site with €7.3M investment.
Promising applications for targeted delivery may be cresting the horizon.
Pharma’s leveraging real-world evidence to drive product approval, reimbursement, and market access.
FDA’s hybrid inspection model will remain a regular means for supplementing onsite inspections and will be further integrated into the agency’s oversight operations.
GSK has completed its demerger of Haleon and has signed an agreement to help support future pandemic preparedness in Europe.
How can we fix the quality manufacturing issues that come with product shortages?
August 01, 2022
DuPont’s new manufacturing site will expand its biopharmaceutical tubing manufacturing capabilities.
The United States has agreed to purchase 66 million doses of Moderna’s bivalent COVID-19 booster candidate for $1.74 billion.
The European Commission has approved Rinvoq (upadacitinib) for treatment of active non-radiographic axial spondyloarthritis.
The European Commission has granted marketing authorization to Upstaza (eladocagene exuparvovec) for treatment of aromatic L-amino acid decarboxylase (AADC) deficiency.