Marksans Pharma Limited has announced that UK MHRA has granted Market Authorisation to the Company s wholly owned subsidiary Relonchem Limited for Fluoxetine 20mg/5ml Oral Solution.
The Drug Controller General of India (DCGI ) has approved market authorisation to COVID-19 vaccine Covovax as a heterologous booster dose for adults who have been administered two doses of Covishield or Covaxin, official sources said on Monday. DCGI Approves Market Authorisation for SII’s COVID-19 Vaccine ‘Covovax’ As Heterologous Booster Dose.
FDA builds capacity of Rwanda counterparts ghanaiantimes.com.gh - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from ghanaiantimes.com.gh Daily Mail and Mail on Sunday newspapers.
Takeda UK Ltd. is pleased to announce that NICE has recommended the use of Revestive ? (teduglutide) once daily subcutaneous injection as an option for people living with Short Bowel Syndrome
The market authorisation of two Covid vaccines - Covaxin and Covishield, given by drug regulator Drug Controller General of India is the subject to the condition of submission of ongoing clinical trial data and safety data of the vaccines, the .