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Novartis Gilenya gets FDA nod

Novartis claimed that the FDA approval makes Gilenya the first oral treatment indicated for relapsing forms of MS available in the US. Gilenya belongs to a new class

Almac passes joint GCP-GMP MHRA inspection

The MHRA inspection was conducted on the GMP side to determine whether Almac’s IXRS integrated phone and web response system was able to adequately ensure that expired products

Novartis unveils SOM230 Phase III study results

PASPORT-CUSHINGS (PASireotide clinical trial PORTfolio – CUSHING’S disease), a randomised study to evaluate a medical therapy in patients with Cushing’s disease, is part of a large-scale global clinical