Zobrazeno 1 - 10
of 86
pro vyhledávání: '"G. Rautmann"'
Autor:
L, Findlay, T, Desai, A, Heath, S, Poole, M, Crivellone, W, Hauck, M, Ambrose, T, Morris, A, Daas, G, Rautmann, K H, Buchheit, J M, Spieser, E, Terao
Publikováno v:
Pharmeuropa bioscientific notes. 2015
An international collaborative study was organised jointly by the World Health Organization (WHO)/National Institute for Biological Standards and Control (NIBSC), the United States Pharmacopeia (USP) and the European Directorate for the Quality of Me
Autor:
Olivier Garraud, Rut Norda, C. Martin, G. Rautmann, S. MacLennan, M. Bagge Hansen, Antoine Haddad
Publikováno v:
Transfusion Clinique et Biologique. 24:34-35
Allergy accounts to near 0.5% of all reported transfusion adverse events. The responsibility of blood components themselves and – therefore – of blood donors is still questioned. The European Community undertook a large international survey to ad
Publikováno v:
Pharmeuropa bioscientific notes. 2014
Following the heparin adulteration crisis, the European Pharmacopoeia (Ph. Eur.) Group of Experts on Biologicals (Group 6) considered a revision of the general chapter 2.7.5. Assay of heparin with regard to the assay of the anticoagulant activity of
Publikováno v:
Vox Sanguinis. 83:42-50
Background and Objectives The disadvantages of autoanalyser methodology for anti-D potency estimation have prompted the search for an alternative reference method. The aim of this study was to carry out a direct comparison of autoanalyser methodology
Publikováno v:
Pharmeuropa bioscientific notes. 2013
An international collaborative study was organised to establish the World Health Organization (WHO) 3(rd) International Standard (IS) for neomycin. Ten laboratories from different countries participated in the collaborative study. The potency of the
Publikováno v:
Pharmacy and Pharmacology Communications. 5:61-66
Publikováno v:
Pharmeuropa bioscientific notes. 2013
An international collaborative study was carried out for the establishment of replacement batches for the European Pharmacopoeia (Ph. Eur.) Somatropin Chemical Reference Substance (CRS) batch 2. The study was organised within the framework of the Bio
Publikováno v:
Pharmeuropa bioscientific notes. 2012
An international collaborative study was organised to establish the World Health Organization (WHO) 3rd International Standard (IS) for dihydrostreptomycin. Eleven laboratories from different countries participated in the collaborative study. The pot
Publikováno v:
Pharmeuropa bioscientific notes. 2011(2)
An international collaborative study has been organised by the European Directorate for the Quality of MedicinesHealthCare (EDQM) to establish the World Health Organization (WHO) 2nd International Standard (IS) for Vancomycin. Twelve laboratories fro
Publikováno v:
Analytical Biochemistry. 213:40-48
Recombinant DNA technology has been widely used for the production of proteins in recent years. In this paper, we describe the expression and the purification of two specific peptides corresponding to parts of the human immunodeficiency virus Rev pro