List of acronyms and abbreviations used in CVMP agenda and minutes
Submitted by Anonymous (not verified) on 18 December 2023 - 14:15
List of acronyms and abbreviations used in CVMP agenda and minutes
Regulatory requirements for the development of medicinal products for Acute Kidney Injury (AKI) - Scientific guideline
Submitted by Anonymous (not verified) on 18 December 2023 - 13:42
Regulatory requirements for the development of medicinal products for Acute Kidney Injury (AKI) - Scientific guideline
Shortage of Abraxane (paclitaxel)
Submitted by Anonymous (not verified) on 18 December 2023 - 12:59
Shortage of Abraxane (paclitaxel)
Multi-annual artificial intelligence workplan 2023-2028 - HMA / EMA joint Big Data Steering Group
Submitted by Anonymous (not verified) on 18 December 2023 - 12:55
Multi-annual artificial intelligence workplan 2023-2028 - HMA / EMA joint Big Data Steering Group
ADHD medicines (atomoxetine, methylphenidate, lisdexamfetamine) supply shortage
Submitted by Anonymous (not verified) on 18 December 2023 - 12:33
ADHD medicines (atomoxetine, methylphenidate, lisdexamfetamine) supply shortage
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes
Submitted by Anonymous (not verified) on 18 December 2023 - 12:33
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure: document with tracked changes
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
Submitted by Anonymous (not verified) on 18 December 2023 - 12:32
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes
Submitted by Anonymous (not verified) on 18 December 2023 - 12:23
European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes
European Medicines Agency post-authorisation procedural advice for users of the centralised procedure
Submitted by Anonymous (not verified) on 18 December 2023 - 12:20
European Medicines Agency post-authorisation procedural advice for users of the centralised procedure
Annex to Letter of Intent (pre-submission request form)
Submitted by Anonymous (not verified) on 18 December 2023 - 12:19
Annex to Letter of Intent (pre-submission request form)