Einhaltung von Metallgrenzwerten in pharmazeutischen Prozessen

Author:

Forfar Laura C.,Murray Paul M.

Publisher

Springer International Publishing

Reference71 articles.

1. ICH Harmonised Guideline (2014) Guideline for elemental impurities, Q3D, current step 4 version. In: International conference on harmonisation of technical. requirements for registration of pharmaceuticals for human use. https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q3D/Q3D_Step_4.pdf. Zugegriffen: 22 Jan 2018

2. Hübner S, De Vries JG, Farina V (2016) Why does industry not use immobilized transition metal complexes as catalysts? Adv Synth Catal 358:3–25. https://doi.org/10.1002/adsc.201500846

3. Buitrago Santanilla A, Regalado EL, Pereira T et al (2015) Nanomole-scale high-throughput chemistry for the synthesis of complex molecules. Science 347:49–53

4. Box GEP, Hunter JS, Hunter WG (2005) Statistics for experimenters. 2nd edn. Wiley, New York

5. Leardi R (2009) Experimental design in chemistry: a tutorial. Anal Chim Acta 652:161–172. https://doi.org/10.1016/j.aca.2009.06.015

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