Pfizer has asked the US Supreme Court of Alabama to reconsider its decision of 4 January 2013, which would allow generics patients to sue brand-name drugmakers.
- INICIO
 - 
                                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
 
 - 
                                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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