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Regulatory
Manufacturing
GMP
Quality assurance
R&D
API
Excipients
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Regulatory
Page 2
Regulatory
Data and AI in medicines regulation, the workplan to 2028
Giuliana Miglierini
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19 June 2025
AUDA-NEPAD is the new PIC/S associated partner
staff
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17 April 2025
Towards the implementation of the electronic product information
Manuele Cantù
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22 January 2025
New procedures for filing post-authorisation variations published by EMA
Manuele Cantù
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28 November 2024
The WHO approved the amendments to the International Health Regulations
Manuele Cantù
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10 July 2024
The EMRN designated as a WHO Listed Authority
Manuele Cantù
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27 June 2024
The EU Commission proposal for the revision of the Variations Regulation
Manuele Cantù
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4 April 2024
Unitary SPC, the EU Parliament approved its position
Manuele Cantù
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28 March 2024
New partners for Darwin EU
Giuliana Miglierini
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21 March 2024
The creation of the African Medicines Agency
Manuele Cantù
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8 February 2024
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