The European Medicines Agency (EMA) has announced that they have recommended the suspension of generic drug approvals and drug applications of over 300 drugs. This is due to unreliable bioequivalence studies carried out by the Indian contract research firm Micro Therapeutic Research Labs.
- INICIO
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                                Genéricos 
                                                                
Novedades
- FDA approves generic teriparatide and levetiracetam
 - US generics launch and approval for Dr Reddy’s and Lupin
 - Five Chinese companies join UN’s MPP for Covid-19 medicines
 - South Korean companies to make generic Bridion and COVID-19 drugs
 
Investigación
- Japan’s drug shortage crisis: challenges and policy solutions
 - Saudi FDA drug approvals and GMP inspections: trend analysis
 - Generic medications in the Lebanese community: understanding and public perception
 - Community pharmacists’ understanding of generic and biosimilar drugs: Lebanon case study
 
General
- Crecimiento de medicamentos genéricos en Brasil y Venezuela
 - EMA launches European shortages monitoring platform to tackle persistent medicine shortages
 - Penetración de los medicamentos genéricos en México y Brasil
 - FDA releases one-year progress report for the Generic Drug Cluster
 
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                                Biosimilares 
                                                                
Novedades
- FDA approves six denosumab biosimilars
 - EMA recommends approval for four biosimilars targeting three therapies
 - FDA approves first interchangeable rapid-acting insulin biosimilar, Kirsty
 - ANVISA approves ranibizumab and tocilizumab biosimilars
 
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