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A G J Daas

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Vero Cells

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Publications

TOP 3
M Girard; B Lorbetskie; G Rautmann; E Terao; A G J Daas; M-A Joly
International collaborative study for the calibration of the Ph. Eur. Somatropin Chemical Reference Substance Batches 3 and 4 (BSP108).
G Rautmann; A G J Daas; KH Buchheit
Collaborative study for the establishment of the 3rd international standard for dihydrostreptomycin.
E Sandberg; A Costanzo; A G J Daas; KH Buchheit
Calibration of the human immunoglobulin BRPs for ACA and molecular size (batch 1) and for Fc function and molecular size (batches 1 & 2).

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All Publications

2013: M Girard; B Lorbetskie; G Rautmann; E Terao; A G J Daas; M-A Joly
International collaborative study for the calibration of the Ph. Eur. Somatropin Chemical Reference Substance Batches 3 and 4 (BSP108).
Pharmeuropa bio & scientific notes 2013;2013():1-39.
2012: G Rautmann; A G J Daas; KH Buchheit
Collaborative study for the establishment of the 3rd international standard for dihydrostreptomycin.
Pharmeuropa bio & scientific notes 2012;2012():16-38.
2012: E Sandberg; A Costanzo; A G J Daas; KH Buchheit
Calibration of the human immunoglobulin BRPs for ACA and molecular size (batch 1) and for Fc function and molecular size (batches 1 & 2).
Pharmeuropa bio & scientific notes 2012;2012():1-15.
2011: John M Wood; E Montomoli; Robert W Newman; A G J Daas; KH Buchheit; E Terao
Collaborative study on influenza vaccine clinical trial serology - part 2: reproducibility study.
Pharmeuropa bio & scientific notes 2011;2011(1):36-54.
2011: John M Wood; Robert W Newman; A G J Daas; E Terao; KH Buchheit
Collaborative study on influenza vaccine clinical trial serology - part 1: CHMP compliance study.
Pharmeuropa bio & scientific notes 2011;2011(1):27-35.
2011: Robert Tierney; J Hockley; Peter Rigsby; E Terao; A G J Daas; KH Buchheit; Dorothea Sesardic
Calibration of the Ph. Eur. Biological Reference Preparation (BRP) for tetanus vaccine (adsorbed) batch 3.
Pharmeuropa bio & scientific notes 2011;2011(1):1-26.
2010: G Rautmann; E Charton; A G J Daas; K-H Buchheit
Collaborative study for the establishment of the third international standard for nystatin.
Pharmeuropa bio & scientific notes 2010;2010(2):68-85.
2010: G Rautmann; A G J Daas; K-H Buchheit
Collaborative study for the establishment of the second international standard for gramicidin.
Pharmeuropa bio & scientific notes 2010;2010(2):56-67.
2010: B Krämer; L Bruckner; A G J Daas; C Milne
Collaborative study for validation of a serological potency assay for rabies vaccine (inactivated) for veterinary use.
Pharmeuropa bio & scientific notes 2010;2010(2):37-55.
2010: E Terao; A G J Daas; G Rautmann; K-H Buchheit
Collaborative study for the establishment of replacement batches of heparin low- molecular-mass for assay biological reference preparations.
Pharmeuropa bio & scientific notes 2010;2010(2):30-6.
2010: S Gross; S W J Janssen; B de Vries; E Terao; A G J Daas; KH Buchheit
Collaborative study for the validation of alternative in vitro potency assays for human tetanus immunoglobulins.
Biologicals : journal of the International Association of Biological Standardization 2010;38(4):501-10.
2010: D Xing; A Maes; Marie-Emmanuelle BEHR-GROSS; A Costanzo; A G J Daas; KH Buchheit
Collaborative study for the standardisation of the histamine sensitizing test in mice and the CHO cell-based assay for the residual toxicity testing of acellular pertussis vaccines.
Pharmeuropa bio & scientific notes 2010;2010(1):51-63.
2010: Johannes Dodt; A Costanzo; A G J Daas; Andreas Hunfeld; KH Buchheit
Calibration of human coagulation factor VII concentrate Ph. Eur. BRP batch 2.
Pharmeuropa bio & scientific notes 2010;2010(1):31-8.
2010: G Rautmann; A G J Daas; K-H Buchheit
Collaborative study for the establishment of the second international standard for amphotericin B.
Pharmeuropa bio & scientific notes 2010;2010(1):1-13.
2009: S Gross; S W J Janssen; B de Vries; E Terao; A G J Daas; KH Buchheit
Collaborative study for the validation of alternative in vitro potency assays for human tetanus immunoglobulin.
Pharmeuropa bio & scientific notes 2009;2009(1):11-25.
2007: Marie-Emmanuelle BEHR-GROSS; A G J Daas; C Burns; A F Bristow
Collaborative study for the establishment of erythropoietin BRP batch 3.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2007;2007(1):49-66.
2007: S Muñoz Botella; JM Spieser; A G J Daas
Market surveillance study on general method 2.9.40. uniformity of dosage units, carried out by the OMCL Network of the EDQM/Council of Europe.
Pharmeuropa scientific notes 2007;2007(1):21-32.
2006: R Winsnes; Dorothea Sesardic; A G J Daas; Marie-Emmanuelle BEHR-GROSS
Collaborative study for the validation of serological methods for potency testing of diphtheria toxoid vaccine (part 2).
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2006;2006(1):73-88.
2006: C Milne; A G J Daas
Establishment of European pharmacopoeia Mycoplasma reference strains.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2006;2006(1):57-72.
2006: E Sandberg; A G J Daas; Marie-Emmanuelle BEHR-GROSS
Collaborative study to establish human immunoglobulin BRP batch 3 and human immunoglobulin (molecular size) BRP batch 1.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2006;2006(1):37-48.
2006: A G J Daas; B Rafferty; Marie-Emmanuelle BEHR-GROSS
Collaborative study for the establishment of replacement batches for somatropin CRS batch 1.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2006;2006(1):23-36.
2006: Johannes Dodt; Andreas Hunfeld; A G J Daas; KH Buchheit
Establishment of the human coagulation factor VII concentrate European Pharmacopoeia biological reference preparation batch 1.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2006;2006(1):15-22.
2005: Sylvie Morgeaux; C Milne; A G J Daas
Feasibility study to develop a common in vitro D antigen assay for inactivated poliomyelitis vaccines.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2005;2005(1):19-26.
2005: Colin Longstaff; Marie-Emmanuelle BEHR-GROSS; A G J Daas; F Lackner
Collaborative study to establish a new biological reference preparation for prekallikrein activator.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2005;2005(1):1-12.
2005: Colin Longstaff; Marie-Emmanuelle BEHR-GROSS; A G J Daas; F Lackner
An international collaborative study to replace the 1st international standard for prekallikrein activator.
Vox sanguinis 2005;88(2):143-51.
2004: Marie-Emmanuelle BEHR-GROSS; A G J Daas; A F Bristow
Collaborative study for the establishment of erythropoietin BRP batch 2.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2004(1):23-33.
2004: A G J Daas; C Milne
Establishment of batch 4 of the Biological Reference Preparation (BRP) for rabies vaccine (inactivated) for veterinary use.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2004(1):17-22.
2004: Ivo Claassen; Riks Maas; Hok Oei; A G J Daas; C Milne
Validation study to evaluate the reproducibility of a candidate in vitro potency assay of newcastle disease vaccines and to establish the suitability of a candidate biological reference preparation.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2004(1):1-15.
2004: R Dobbelaer; A G J Daas; C Milne
Establishment of European Pharmacopoeia (Ph. Eur.) Biological Reference Preparations (BRP) batch 2 for rDNA hepatitis B vaccine (method A and B).
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2003(2):77-90.
2004: R Winsnes; Dorothea Sesardic; A G J Daas; Marie-Emmanuelle BEHR-GROSS
Collaborative study for the validation of serological methods for potency testing of diphtheria toxoid vaccines-part 1.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2003(2):35-68.
2004: C Micha Nübling; A G J Daas; KH Buchheit
Collaborative study for establishment of a European Pharmacopoei Biological Reference Preparation (BRP) for B19 virus DNA testing of plasma pools by nucleic acid amplification technique.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2003(2):27-34.
2004: E Charton; A G J Daas; J Sandrin; J H McB Miller
Collaborative studies for the establishment of reference substances for the microbiological assay of antibiotics.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2004;2003(2):1-8.
2003: Ivo Claassen; Riks Maas; A G J Daas; C Milne
Feasibility study to evaluate the correlation between results of a candidate in vitro assay and established in vivo assays for potency determination of Newcastle disease vaccines.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2003;2003(1):51-66.
2003: F Fuchs; P Minor; A G J Daas; C Milne
Establishment of European Pharmacopoeia BRP batch 2 for inactivated poliomyelitis vaccine for in vitro D antigen assay.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2003;2003(1):23-50.
2003: Dorothea Sesardic; C Prior; A G J Daas; KH Buchheit
Collaborative study for establishment of the European Pharmacopoeia BRP batch 1 for diphtheria toxin.
Pharmeuropa bio / the Biological Standardisation Programme, EDQM 2003;2003(1):5-21.
2002: KH Buchheit; A G J Daas
Establishment of the European Pharmacopoeia Biological Reference Preparation (Ph. Eur. BRP) for hepatitis A vaccine type B (Aventis Pasteur) batch 2.
Pharmeuropa. Special issue biologicals 2002;2002(1):95-108.
2002: KH Buchheit; A G J Daas; J Stalder
Collaborative study for the establishment of the Ph. Eur. BRP for oral poliomyelitis vaccine (OPV) Batch 3 for use in the potency assay.
Pharmeuropa. Special issue biologicals 2002;2002(1):67-91.
2002: N Kirschbaum; L Wood; Peter A Lachenbruch; M Weinstein; A G J Daas; G Rautmann; JM Spieser; KH Buchheit
Calibration of the Ph. Eur. BRP Batch 3/Mega 2 (US/FDA) standard for human coagulation factor VIII concentrate for use in the potency assay.
Pharmeuropa. Special issue biologicals 2002;2002(1):31-64.
2002: KH Buchheit; A G J Daas; K H Jönsson
Collaborative study for establishment of an HPLC-method for batch consistency control of recombinant interferon-alfa-2.
Pharmeuropa. Special issue biologicals 2002;2002(1):7-27.
2002: R Lucken; A G J Daas; Marie-Emmanuelle BEHR-GROSS
Collaborative study for the establishment of a European Pharmacopoeia Biological Reference Preparation for Clostridia antiserum for serological potency testing of veterinary clostridial vaccines.
Developments in biologicals 2002;111():171-80.
2002: R Winsnes; Dorothea Sesardic; A G J Daas; Peter Rigsby
A Vero cell method for potency testing of diphtheria vaccines.
Developments in biologicals 2002;111():141-8.
2002: H H Lensing; Marie-Emmanuelle BEHR-GROSS; A G J Daas; JM Spieser
Collaborative study for the establishment of two European Pharmacopoeia Biological Reference Preparations for serological potency testing of tetanus vaccines for veterinary use.
Developments in biologicals 2002;111():69-76.
2001: E Sandberg; A G J Daas; Marie-Emmanuelle BEHR-GROSS
Collaborative study for the establishment of human immunoglobulin European Pharmacopoeia Biological Reference Preparation batch no. 2.
Pharmeuropa. Special issue biologicals 2001;2001(1):27-42.
2001: R Dobbelaer; A G J Daas; Marie-Emmanuelle BEHR-GROSS
Collaborative study for the establishment of a European Pharmacopoeia Biological Reference Preparation for pertussis toxin--Part 1.
Pharmeuropa. Special issue biologicals 2001;2001(1):15-23.
1999: R Winsnes; Coenraad F M Hendriksen; Dorothea Sesardic; A Akkermans; A G J Daas
Serological assays as alternatives to the Ph Eur challenge test for batch release of tetanus vaccines for human use.
Developments in biological standardization 1999;101():277-88.