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Oncology Products in the European Union: An Analysis of Regulatory Approvals with a CHMP Oral Explanation.
Ther Innov Regul Sci. 2021 Sep;55(5):1036-1044. doi: 10.1007/s43441-021-00303-x. Epub 2021 May 26.
Ther Innov Regul Sci. 2021.
PMID: 34041707
Acceptance of stakeholder comments during EMA scientific guideline public consultations: Legitimacy of the quadruple helix model of innovation.
Heikkinen I, Torqui A.
Heikkinen I, et al. Among authors: torqui a.
Br J Clin Pharmacol. 2023 Mar;89(3):1003-1011. doi: 10.1111/bcp.15542. Epub 2022 Oct 9.
Br J Clin Pharmacol. 2023.
PMID: 36129994
Free article.
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Regional Differences During the ICH Regulatory Consultation Process Between the EU, US, and Japan.
Torqui A, Macau AM.
Torqui A, et al.
Ther Innov Regul Sci. 2018 Jul;52(4):438-441. doi: 10.1177/2168479017744199. Epub 2017 Dec 20.
Ther Innov Regul Sci. 2018.
PMID: 29714552
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[Five years of European regulation on medication use in children: what has been achieved?].
van den Berg H, Torqui A, Wesseling AI.
van den Berg H, et al. Among authors: torqui a.
Ned Tijdschr Geneeskd. 2013;157(38):A6000.
Ned Tijdschr Geneeskd. 2013.
PMID: 24330788
Dutch.
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