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NCF International
Regulatory
Manufacturing
GMP
Quality assurance
R&D
API
Excipients
Trials
Drug Delivery
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Regulatory
Page 4
Regulatory
The closing report of the EMA and European Commission (EC) action...
Manuele Cantù
-
30 March 2023
MHRA, approval via the ECDRP route will continue for all 2023
Manuele Cantù
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9 March 2023
The CTIS has fully entered into force
Manuele Cantù
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8 February 2023
Main legal barriers to the better use of health data for...
Caterina Lucchini
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14 February 2019
Regulatory science strategy to 2025, open consultations
Caterina Lucchini
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21 January 2019
Ema: patient records and real world data for clinical studies on...
Caterina Lucchini
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10 January 2019
Clinical trials. Two years of PRIME
Cristiana Bernini
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14 June 2018
Operation Management: an integrated vision for a better efficiency of the...
14 April 2017
The Italian Medicines Agency Aifa announced the new Fast Track procedure...
Giuliana Miglierini
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19 December 2016
European policy. The Trade Secrets Directive
Cristiana Bernini
-
17 June 2016
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