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