Long-standing issues result in warning letter for Teva
Repeat observations for Teva’s facility results in US FDA issue warning letter, citing ‘inadequate oversight and control by executive management’.
Repeat observations for Teva’s facility results in US FDA issue warning letter, citing ‘inadequate oversight and control by executive management’.
The US Government released its fiscal year 2020 budget plan, which addressed affordable prescription drug costs through increased generic competition.
NEWS IN BRIEF
Sagent purchases Xellia’s FDA-approved site in North Carolina, which has capabilities to manufacture both small molecule and biologic products.
Sinclair Research and Turner Scientific sign an exclusive partnership through which the preclinical CROs will offer GLP ototoxicity testing services.
Clinerion gains first Poland-based partner as Szpital Specjalistyczny w Brzozowie joins the global hospital network to bolster data integration.
CRF Bracket closes its first full quarter as a combined entity with more than a 20% increase in new clinical trial business – and will “aggressively look for partners” from its current and future customers, says CEO.
Drug development advisory firm Rosa & Co. enters research agreement with Chugai pharmaceutical to provide access to PhysioPD research services for translational biology.