Latest Updates

The company has has received Emergency Use Authorization (EUA) by the US Food and Drug Administration for its TaqPathCOVID-19…

The inspection for the facility was carried out between February 10, 2020 and February 14, 2020 and concluded with no observations

There is significant interest in HMO use as a dietary supplement and potentially in food and beverage and pet food applications,…

New studies show NDMA impurity increases in some meds over time, and when stored at higher than room temperature

In September 2018, Aurobindo Pharma had said its US subsidiary has entered into a pact to acquire commercial operations and three…

The study, completed in the first attempt, was conducted over a period of 15 months at over 100 sites in the US enrolling 1,400…

Vaccination for pneumococcal disease was only introduced in children in late 2017 across three Indian states, and vaccination in…

Dealing with hampered production and lack of input raw materials, AGI glaspac has put in measures to cushion the blow. For…

Koki Sato, a seasoned biopharmaceutical leader with over 17 years of experience across geographies has been assigned as the new…

The Inspection has been closed with a “VAI” (Voluntary Action Indicated) classification in the EIR, for the three observations…