EMA

Summary : First-ever lentiviral hematopoietic stem cell gene therapy approved for reimbursement by NHS England Two children with early-onset MLD recently treated…

Summary : EMA’s human medicines committe  has recommended granting  conditional marketing authorisation for the oral antiviral medicine Paxlovid (PF-07321332 / ritonavir) for…

Summary : There is currently no cure for cystic fibrosis (CF), a debilitating, progressive condition with over 10,830 people in the UK…

Synopsis: EMA has started evaluating an application for a conditional marketing authorisation for the oral antiviral medicine Paxlovid (PF-07321332 and ritonavir). The…

Synopsis: Bharat Biotech on Monday informed that India has supplied another batch of humanitarian assistance consisting of 5,00,000 doses of COVID-19 vaccine,…

Synopsis: The EMA’s human medicines committee has said it cannot approve Biogen and Eisai’s Alzheimer’s disease therapy Aduhelm, saying it was unconvinced…

Synopsis- India-made Covovax on Friday became the ninth Covid-19 vaccine to receive WHO’s emergency use listing approval, with manufacturer Serum Institute of…

Summary – The European Medicines Agency (EMA) has issued a list of about 100 regulatory science topics that need further research to close…