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Regulatory
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MHRA, approval via the ECDRP route will continue for all 2023
Manuele Cantù
-
9 March 2023
0
The CTIS has fully entered into force
Manuele Cantù
-
8 February 2023
0
Main legal barriers to the better use of health data for...
Caterina Lucchini
-
14 February 2019
0
Regulatory science strategy to 2025, open consultations
Caterina Lucchini
-
21 January 2019
0
Ema: patient records and real world data for clinical studies on...
Caterina Lucchini
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10 January 2019
0
Clinical trials. Two years of PRIME
Cristiana Bernini
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14 June 2018
0
Operation Management: an integrated vision for a better efficiency of the...
staff
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14 April 2017
0
The Italian Medicines Agency Aifa announced the new Fast Track procedure...
Giuliana Miglierini
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19 December 2016
0
European policy. The Trade Secrets Directive
Cristiana Bernini
-
17 June 2016
0
3D printing. Waiting for specific rules to print devices
Cristiana Bernini
-
6 April 2016
0
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