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Refinado por: data de publicação: Information Technology remover assunto: ind remover
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1
Pre-clinical safety and toxicology profile of a candidate vaccine to treat oxycodone use disorder
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Artigo
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Pre-clinical safety and toxicology profile of a candidate vaccine to treat oxycodone use disorder

Hamid, Fatima A. ; Marker, Cheryl L. ; Raleigh, Michael D. ; Khaimraj, Aaron ; Winston, Scott ; Pentel, Paul R. ; Pravetoni, Marco

Vaccine, 2022-05, Vol.40 (23), p.3244-3252 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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2
De las nanotecnologías a la industria 4.0: una evolución de términos
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Artigo
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De las nanotecnologías a la industria 4.0: una evolución de términos

Foladori, Guillermo ; Ortiz-Espinoza, Ángeles

Nómadas, 2022-04 (55), p.63-73 [Periódico revisado por pares]

Bogota: Fundacion Universidad Central

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3
Regulation and status of herbal medicine clinical trials in Korea
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Artigo
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Regulation and status of herbal medicine clinical trials in Korea

Lee, Boram ; Choi, Yujin ; Kim, Pyung-Wha ; Yang, Changsop ; Lee, Myeong Soo

Integrative medicine research, 2021-06, Vol.10 (2), p.100688, Article 100688 [Periódico revisado por pares]

Elsevier B.V

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4
Retrospective evaluation of single patient investigational new drug (IND) requests in pediatric oncology
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Artigo
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Retrospective evaluation of single patient investigational new drug (IND) requests in pediatric oncology

Shulman, David S. ; Kiwinda, Lulla V. ; Edwards, Stacey ; Clinton, Catherine M. ; Hunt, Sarah ; Greenspan, Lianne ; Lawler, Kristen D. ; Reaman, Gregory ; Al‐Sayegh, Hasan ; Bona, Kira ; O'Neill, Allison F. ; Shusterman, Suzanne ; Janeway, Katherine A. ; Place, Andrew E. ; Chi, Susan N. ; Ma, Clement ; DuBois, Steven G.

Cancer medicine (Malden, MA), 2021-04, Vol.10 (7), p.2310-2318 [Periódico revisado por pares]

United States: John Wiley & Sons, Inc

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5
Regulatory considerations for developing a phase I investigational new drug application for autologous induced pluripotent stem cells‐based therapy product
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Artigo
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Regulatory considerations for developing a phase I investigational new drug application for autologous induced pluripotent stem cells‐based therapy product

Jha, Balendu Shekhar ; Farnoodian, Mitra ; Bharti, Kapil

Stem cells translational medicine, 2021-02, Vol.10 (2), p.198-208 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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6
Regulatory Framework for Academic Investigator-Sponsored Investigational New Drug Development of Cell and Gene Therapies in the USA
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Artigo
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Regulatory Framework for Academic Investigator-Sponsored Investigational New Drug Development of Cell and Gene Therapies in the USA

Dasgupta, Anindya ; Herzegh, Kristen ; Spencer, H. Trent ; Doering, Christopher ; Day, Eric ; Swaney, William P.

Current stem cell reports, 2021, Vol.7 (4), p.129-139 [Periódico revisado por pares]

Cham: Springer International Publishing

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7
Interface of Building Information Modeling and Blueprints on Construction Sites
Material Type:
Tese
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Interface of Building Information Modeling and Blueprints on Construction Sites

Johannessen, Stian Bråten

University of Agder 2021

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8
Use of 55 PET radiotracers under approval of a Radioactive Drug Research Committee (RDRC)
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Use of 55 PET radiotracers under approval of a Radioactive Drug Research Committee (RDRC)

Jackson, Isaac M. ; Lee, So Jeong ; Sowa, Alexandra R. ; Rodnick, Melissa E. ; Bruton, Laura ; Clark, Mara ; Preshlock, Sean ; Rothley, Jill ; Rogers, Virginia E. ; Botti, Leslie E. ; Henderson, Bradford D. ; Hockley, Brian G. ; Torres, Jovany ; Raffel, David M. ; Brooks, Allen F. ; Frey, Kirk A. ; Kilbourn, Michael R. ; Koeppe, Robert A. ; Shao, Xia ; Scott, Peter J. H.

EJNMMI radiopharmacy and chemistry, 2020-11, Vol.5 (1), p.24-16, Article 24 [Periódico revisado por pares]

Cham: Springer International Publishing

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9
Current System of Overseeing Drug Trials in Developing Countries by the FDA Is Dangerous
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Artigo
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Current System of Overseeing Drug Trials in Developing Countries by the FDA Is Dangerous

White, C. Michael

The Annals of pharmacotherapy, 2020-09, Vol.54 (9), p.928-932 [Periódico revisado por pares]

Los Angeles, CA: SAGE Publications

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10
An FDA analysis of clinical hold deficiencies affecting investigational new drug applications for oncology products
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Artigo
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An FDA analysis of clinical hold deficiencies affecting investigational new drug applications for oncology products

Manning, Michael L. ; Thompson, Matthew D. ; Saber, Haleh ; Maher, Virginia E. ; Crich, Joyce Z. ; Leighton, John K.

Regulatory toxicology and pharmacology, 2020-02, Vol.110, p.104511, Article 104511 [Periódico revisado por pares]

Netherlands: Elsevier Inc

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