BioWorld. Link to homepage.
BioWorld
BioWorld Science
BioWorld Asia
Data Snapshots
Biopharma
Medical technology
Infographics: Dynamic digital data analysis
Index insights
NME Digest
Special reports
Infographics: Dynamic digital data analysis
Trump administration impacts
Med-tech outlook 2026
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 - Saturday, May 2, 2026
Home
»
Topics
»
Regulatory
» EMA
EMA
RSS
EMA committee begins safety review of Diane-35 and generics
Feb. 11, 2013
EMA grants accelerated assessment to trametinib application
Feb. 8, 2013
EMA approves label extension for Abilify
Feb. 6, 2013
French ANSM to suspend marketing of Diane-35 and generics for acne
Jan. 31, 2013
Prosensa's Duchenne muscular dystrophy products achieve orphan drug status
Jan. 30, 2013
Novartis receives positive CHMP opinion for Ilaris in acute gouty arthritis
Jan. 22, 2013
EMA confirms recommendation to suspend nicotinic acid/laropiprant
Jan. 21, 2013
CHMP recommends approval of Jetrea in Europe for vitreomacular traction
Jan. 21, 2013
Bosutinib receives positive CHMP opinion for conditional marketing authorization
Jan. 21, 2013
European CHMP set to discuss MAA for defibrotide
Jan. 18, 2013
Previous
1
2
…
104
105
106
107
108
109
110
111
112
…
159
160
Next