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Items where Author is "Borchard, Gerrit"

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Number of items: 7.

2019

Flühmann, Beat and Ntai, Ioanna and Borchard, Gerrit and Simoens, Steven and Mühlebach, Stefan. (2019) Nanomedicines: The magic bullets reaching their target? European journal of pharmaceutical sciences, 128. pp. 73-80.

2017

Hussaarts, Leonie and Mühlebach, Stefan and Shah, Vinod P. and McNeil, Scott and Borchard, Gerrit and Flühmann, Beat and Weinstein, Vera and Neervannan, Sesha and Griffiths, Elwyn and Jiang, Wenlei and Wolff-Holz, Elena and Crommelin, Daan J. A. and de Vlieger, Jon S. B.. (2017) Equivalence of complex drug products: advances in and challenges for current regulatory frameworks. Annals of the New York Academy of Sciences, 1407 (1). pp. 39-49.

2016

de Vlieger , Jon S. B. and Borchard, Gerrit and Shah, Vinod P. and Flühmann, Beat and Neervannan, Sesha and Mühlebach , Stefan F.. (2016) Is the EU ready for non-biological complex drug products? Generics and biosimilars initiative journal, 5 (3). pp. 101-102.

2015

Mühlebach , Stefan F. and Shah, Vinod P. and McNeil, Scott E. and Borchard, Gerrit and Weinstein, Vera and de Vlieger , Jon S. B. and Flühmann, Beat and Crommelin, Daan J. A. and Neervannan, Sesha. (2015) NBCDS and their follow-on versions: time for an editorial section (perspective). Generics and Biosimilars Initiative Journal, 4 (4). pp. 167-170.

Mühlebach, Stefan and Borchard, Gerrit and Yildiz, Selcan. (2015) Regulatory challenges and approaches to characterize nanomedicines and their follow-on similars. Nanomedicine (London, England), 10 (4). pp. 659-674.

2014

Tinkle, Sally and McNeil, Scott E. and Mühlebach, Stefan and Bawa, Raj and Borchard, Gerrit and Barenholz, Yechezkel Chezy and Tamarkin, Lawrence and Desai, Neil. (2014) Nanomedicines: addressing the scientific and regulatory gap. Annals of the New York Academy of Sciences [0077-8923], 1313. pp. 35-56.

2012

Borchard, Gerrit and Flühmann, Beat and Mühlebach, Stefan. (2012) Nanoparticle iron medicinal products - Requirements for approval of intended copies of non-biological complex drugs (NBCD) and the importance of clinical comparative studies. Regulatory toxicology and pharmacology, 64 (2). pp. 324-328.

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