BioWorld. Link to homepage.
BioWorld
BioWorld MedTech
BioWorld Asia
BioWorld Science
Data Snapshots
BioWorld
BioWorld MedTech
Infographics: Dynamic digital data analysis
Index insights
NME Digest
Special reports
Infographics: Dynamic digital data analysis
Trump administration impacts
Under threat: mRNA vaccine research
BioWorld at 35
Biopharma M&A scorecard
Bioworld 2025 review
BioWorld MedTech 2025 review
BioWorld Science 2025 review
Women's health
China's GLP-1 landscape
PFA re-energizes afib market
China CAR T
Alzheimer's disease
Coronavirus
More reports can be found here
BioWorld. Link to homepage.
Sign In
Sign Out
My Account
Subscribe
BioWorld - Thursday, December 25, 2025
Home
»
Topics
»
Regulatory
» EMA
EMA
RSS
Abbott withdraws European MAA for Ozespa
Jan. 19, 2011
ChemGenex notifies EMA of withdrawal of MAA for Tekinex for Ph+ CML
Jan. 17, 2011
New indication for Lucentis in E.U. for vision loss in diabetic macular edema
Jan. 11, 2011
EMA and FDA grant expedited review for boceprevir
Jan. 11, 2011
Invega approved in E.U. for schizoaffective disorder
Jan. 7, 2011
EMA to review Allos' MAA for Folotyn in relapsed or refractory PTCL
Dec. 28, 2010
Novartis receives E.U. approval for Tasigna in newly diagnosed Ph+ CML
Dec. 27, 2010
CHMP recommends marketing authorization for Janssen-Cilag's Xeplion
Dec. 23, 2010
CHMP recommends a variation to marketing terms for Simponi
Dec. 23, 2010
CHMP recommends approval of Teysuno for treatment of advanced gastric cancer
Dec. 23, 2010
Previous
1
2
…
132
133
134
135
136
137
138
139
140
…
158
159
Next