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Marksans Pharma Ltd announces UK MHRA approval for Fluoxetine 20mg/5ml Oral Solution

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.

DCGI Approves Market Authorisation for SII s COVID-19 Vaccine Covovax As Heterologous Booster Dose

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

FDA builds capacity of Rwanda counterparts
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