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NCF International
Regulatory
Manufacturing
GMP
Quality assurance
R&D
API
Excipients
Trials
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Regulatory
Page 4
Regulatory
EMA opens the early dialogue to the development of anti-infective therapeutics
Giuliana Miglierini
-
19 June 2019
EMA’s vision on evidence by design to evaluate the added therapeutic...
Giuliana Miglierini
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15 May 2019
The EURIPID Collaboration for pricing and reimbursement
Giuliana Miglierini
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16 April 2019
EMA’s first guideline on medical devices integral to medicinal products
Giuliana Miglierini
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21 March 2019
Consultation on the future of Regulatory Sciences to 2025
Giuliana Miglierini
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20 February 2019
New Q&As on safety features from the EU Commission
Giuliana Miglierini
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15 January 2019
EMA opened a consultation on the use of patient registries for...
Giuliana Miglierini
-
11 December 2018
The use of real world data for R&D of pharmaceuticals
Giuliana Miglierini
-
21 November 2018
Brexit: EU Commission warns on possible issues regarding clinical trials
Giuliana Miglierini
-
23 October 2018
Regulators launched activities to prepare for the Brexit
Giuliana Miglierini
-
20 September 2018
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