EMA starts review of sodium oxybate in alcohol dependence
FDA approves removal of REMS programs within Bristol Myers Squibb’s cell therapy labels
European Commission approves Eylea 8 mg with extended 6-month treatment interval for nAMD and visual impairment due to DME
Shukra Pharmaceuticals receives LoA from RMSCL
Lupin launches Prucalopride tablets in US
SMS Pharmaceuticals completes USFDA inspection at Central Laboratory Analytical Services
Star Health Insurance partners with Medi Assist to transform claims through AI and Digital Innovation
Biocon Biologics receives Health Canada approval for Yesafili
Teijin Pharma receives approval for additional indication for XEOMIN in Japan
Ashland expands viatel bioresorbable polymers offering for medical devices
The company's decision to withdraw the MAA was due to the timing of the availability of Chemistry Manufacturing and Controls
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