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Aurelie Mahalatchimy
Aurelie Mahalatchimy
CNRS Permanent researcher, UMR 7318- DICE- CERIC, Aix Marseille University, Toulon University, Pau
Email verificata su univ-amu.fr - Home page
Titolo
Citata da
Citata da
Anno
Are there specific translational challenges in regenerative medicine? Lessons from other fields
J Gardner, A Faulkner, A Mahalatchimy, A Webster
Regenerative Medicine 10 (7), 885-895, 2015
492015
The legal landscape for advanced therapies: material and institutional implementation of European Union rules in France and the United Kingdom
A Mahalatchimy, E Rial‐Sebbag, V Tournay, A Faulkner
Journal of law and society 39 (1), 131-149, 2012
372012
Reimbursement of cell-based regenerative therapy in the UK and France
A Mahalatchimy
Medical law review 24 (2), 234-258, 2016
242016
Human stem cells patents—Emerging issues and challenges in Europe, United States, China, and Japan
AYT Wong, A Mahalatchimy
The Journal of world intellectual property 21 (5-6), 326-355, 2018
202018
Communication of results and disclosure of incidental findings in longitudinal paediatric research
V Anastasova, A Mahalatchimy, E Rial‐Sebbag, JM Anto Boque, T Keil, ...
Pediatric Allergy and Immunology 24 (4), 389-394, 2013
202013
The impact of European embryonic stem cell patent decisions on research strategies
A Mahalatchimy, E Rial-Sebbag, AM Duguet, F Taboulet, ...
Nature Biotechnology 33 (1), 41-43, 2015
142015
Access to advanced therapy medicinal products in the EU: where do we stand?
A Mahalatchimy
European journal of health law 18 (3), 305-317, 2011
132011
Exclusion of patentability of embryonic stem cells in Europe: another restriction by the European Patent Office
A Mahalatchimy, E Rial-Sebbag, M Duguet, A Cambon-Thomsen, ...
European Intellectual Property Review 37 (1), 25-28, 2015
92015
The emerging landscape of reimbursement of regenerative medicine products in the UK: publications, policies and politics
A Mahalatchimy, A Faulkner
Regenerative medicine 12 (6), 611-622, 2017
82017
Framing and legitimating EU legal regulation of human gene-editing technologies: key facets and functions of an imaginary
A Mahalatchimy, PL Lau, P Li, ML Flear
Journal of Law and the Biosciences 8 (2), lsaa080, 2021
72021
The politics of valuation and payment for regenerative medicine products in the UK
A Faulkner, A Mahalatchimy
New Genetics and Society 37 (3), 227-247, 2018
62018
Accreditation and regulations in cell therapy
C Chabannon, O Caunday‐Rigot, C Faucher, I Slaper‐Cortenbach, ...
ISBT Science Series 11 (S1), 271-276, 2016
62016
Les unités de thérapie cellulaire à l’épreuve de la réglementation sur les médicaments de thérapie innovante
C Chabannon, F Sabatier, E Rial-Sebbag, B Calmels, J Veran, ...
médecine/sciences 30 (5), 576-583, 2014
52014
Regulating Medicines in the European Union
A Mahalatchimy
42020
EU law and policy on new health technologies
E Brosset, A Mahalatchimy
Research handbook on EU health law and policy, 197-221, 2017
42017
Does the French Bioethics Law create a'moral exception'to the use of human cells for health? A legal and organizational issue
A Mahalatchimy, E Rial-Sebbag, V Tournay, A Faulkner
Dilemata, 17-37, 2011
42011
Bioethics and European Union: the advanced therapy medicinal products’ case
A Mahalatchimy
Opinio Juris in Compratione 2, 2010
42010
Chapitre 6. Cells’ safety in Europe: Towards an ethical safety
E Rial-Sebbag*, A Mahalatchimy**, AM Duguet***
Journal International de Bioéthique 28 (2), 107-129, 2017
32017
Le monopole pharmaceutique en Grande-Bretagne
A Mahalatchimy
Cahier de Droit de la Santé juridiques, historiques et prospectifs, 109-127, 2017
32017
The European Medicines Agency: a public health European agency
A Mahalatchimy, E Rial-Sebbag, N De Grove-Valdeyron, V Tournay, ...
Med. & L. 31, 25, 2012
32012
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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