Bristol-Myers Squibb selects Cegedim CRM platform
The contract includes an upgrade of all US sales teams to Mobile Intelligence, as well as a suite of implementation and support services. Mobile Intelligence allows for cost-effective
The US Food and Drug Administration (FDA) has granted accelerated approval to Bristol Myers Squibb’s (BMS) Zenbexus (iberdomide), along with daratumumab and hyaluronidase-fihj and dexamethasone (ZDd), to treat adult multiple myeloma (MM) patients.
Verisens PSA is an in-vitro diagnostic assay for the high-sensitivity detection and quantification of prostate specific antigen (PSA), developed in collaboration with the International Institute for Nanotechnology at
Clariant claims that the new Mevopur brand acknowledges the pharmaceutical and medical industry’s need for material consistency, reliability and change-control and can help brand owners and manufacturers minimise