News from the world
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...
latest news
21 Mar
EU pharmaceutical policy: MEPs support comprehensive reform
20 Mar
Riforma farmaceutica: il Parlamento Ue non tocca (quasi) i tempi della tutela regolatoria
15 Mar
US FDA Final Guidance: Controlled Correspondence Related to Generic Drug Development
FDA publishes artificial intelligence paper
14 Mar
Intelligenza artificiale: il Parlamento europeo ha approvato l’Ai Act
13 Mar
Efedrina e pseudoefedrina, nuove regole e sanzioni su export farmaci.
05 Mar
Why, Who, When, Where and More: New Draft Guidance on Notifying US FDA about Discontinuance or Interruption in Manufacturing
28 Feb
AIFA - Francesco Fera facente funzioni alla guida dell'Agenzia
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