News dal mondo
16
Apr
FDA aims for greater use of remote assessments for low-risk facilities
The US Food and Drug Administration (FDA) has conducted more than 20 remote regulatory assessments (RRAs)...
11
Il Parlamento adotta la sua posizione sulla riforma del sistema farmaceutico UE
I deputati hanno adottato le loro proposte per rinnovare la legislazione farmaceutica, promuovere l'innovazione...
09
EDQM - How to identify the manufacturing sites linked to CEP application (revised document)?
Please consult the revised policy document which has been updated to complete the identification...
Does the US Drug Shortage White Paper Fall Short?
The U.S. Department of Health and Human Services (HHS) recently published a White Paper on Policy...
le ultime news
29 Gen
US FDA Issues Revised Draft Guidance on Remote Regulatory Assessments
26 Gen
First court judgment on SPC manufacturing waiver alarms off-patent drugmakers
European Council clears EMA to overhaul its fee system to ensure adequate funding
24 Gen
EMA Revised Drugmaker User Guide for Small, Medium Companies Released
FDA's ISTAND Pilot Program accepts submission of first artificial intelligence-based and digital health technology for neuroscience
European Commission adopts first European positive lists for drinking water
US FDA Draft Guidance on Good Manufacturing Practice for Active Pharmaceutical Ingredients Used in Veterinary Drug Products
23 Gen
EU Commission opens participation to Critical Medicines Alliance
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