The US Food and Drug Administration (FDA) has approved Azurity Pharmaceuticals’ Danziten (nilotinib), the first and only ...

The Food and Drug Administration (FDA) has approved a new presentation of Selarsdi ™ (ustekinumab-aekn), a biosimilar to Stelara ® (ustekinumab), expanding the product’s indications to include ...

Intravital microscopy (IVM) enables live imaging of animals at single-cell level, offering essential insights into cancer progression. This technique allows for the observation of single-cell ...

“Doctor Odyssey,” TV hitmaker Ryan Murphy’s new network medical drama set on a cruise ship, has already featured a syphilis outbreak, a nose falling off a woman’s face, a man overboard, a ...

We observed tasks in the vaccine preparation process, from the time of removal of the vial or the syringe package from the refrigerator until the time it was ready to be administered to a patient.

In April, the FDA approved 45mg/0.5mL and 90mg/mL single-dose prefilled syringes of Selarsdi for subcutaneous injection for the treatment of plaque psoriasis and psoriatic arthritis. The product ...

Selarsdi, a human interleukin-12 and -23 antagonist, was originally approved in April 2024 in a prefilled syringe for subcutaneous use (45mg/0.5mL and 90mg/mL). The indications at the time ...

With the ability to accommodate injection volumes up to 5ml and high-viscosity fluids of up to 1000cP ... minimizing the need for change parts while supporting a wide range of syringe geometries. A ...