Scientific Library: results

Conference

Conference-Webaf 2022

Multiple-Attribute Monitoring in QC: feasibility and alternatives to the bottom up approach

During Waters European Biopharma Analytical Forum 2022 (Webaf), Claire Butré presented on Multiple-Attribute Monitoring in QC

During her talk, she covered the following topics:

Authors
Claire Butré
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Conference_use of octet

Use of Octet in a GMP environment: constraints and applications

Discover more about the use of Octet in a GMP regulated environment.

During this presentation, Arnaud Delobel goes through different subjects:

Authors
Arnaud Delobel
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Quality Assistance 2D-LC/MS

2D-LC/MS workflows for the automated analysis of in-process samples and for the characterization of mAbs in a GMP regulated environment

Discover more about the applications of the 2D-LC/MS at Quality Assistance and how advances in analytical characterisation of mAbs can help you speed up time to market of your biotherapeutics

Authors
Gery Van Vyncht
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Q3D - Elemental Impurities

What implications for APIs & excipients suppliers?
Authors
Philippe De Raeve, Scientific Director
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Publications & Application notes

A new alternative tool to analyse glycosylation in pharmaceutical proteins based on infrared spectroscopy combined with nonlinear support vector regression

Authors
Sabrina Hamla (a)
Pierre-Yves Sacré (a)
Allison Derenne (b)
Kheiro-Mouna Derfoufi (b)
Ben Cowper (c)
Claire I. Butré (d)
Arnaud Delobel (d)
Erik Goormaghtigh (a)
Philippe Hubert (a)
Eric Ziemons (a)
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Development and validation of an antibody-drug conjugate bioassay

Authors
Thomas Henri
Fabian Vandermeers
Vincent Bertholet
Arnaud Delobel
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Fast and accurate absolute quantification of antibodies and antibody-drug conjugate using Isotope Dilution-Triple Quadrupole ICP-MS

Authors
Juliusz Bianga
Philippe De Raeve
Magali Perez
Arnaud Delobel
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Stress testing of Humira (adalimumab) monitored by Hydrogen-Deuterium Exchange Mass Spectrometry (HDX-MS)

Authors
Eric Largy
Arnaud Delobel
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Epitope mapping of an interleukin receptor for three therapeutic antibodies by Hydrogen-Deuterium Exchange Mass Spectrometry (HDX-MS)

Authors
Eric Largy
Caroline Cajot
Arnaud Delobel
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Characterisation of Anti-HCP antibodies by 2D differential Gel Electrophoresis

Authors
Arnaud Delobel
Alix Verret
Nicolas Trinchero
Géry Van Vyncht
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Fast and accurate absolute-quantification of proteins and antibodies using Isotope Dilution-Triple Quadrupole ICP-MS

Authors
Agilent Technologies
Philippe De Raeve
Juliusz Bianga
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Scientific poster

Absolute quantification of proteins & mAbs by ICP-MS

Authors
Julius Bianga
Philippe De Raeve
Arnaud Delobel
Location
Analytical Technologies Europe 2017
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Development and use of 2D-LC/MS as a versatile and powerful tool for the analysis of mAbs and ADCs in a regulated environment

Authors
Eric Largy
Anicet Catrain
Géry Van Vyncht
Arnaud Delobel
Location
Analytical Technologies Europe 2016
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Characterizing Deamidation and Oxidation in Adalimumab with Low pH Peptide Mapping and Middle-Up Mass Spec Analysis.

Authors
Chris Hosfield
Eric Largy
Anicet Catrain
Fabrice Cantais
Géry Van Vyncht
Michael Rosenblatt
Sergei Saveliev
Marjeta Urh
Arnaud Delobel
Location
ASMS Sanibel Conference 2016
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Elemental impurities: how to be compliant with ICH Q3D guideline?

Authors
Philippe De Raeve
Pascal Brichart
Julius Bianga
Géry Van Vyncht
Arnaud Delobel
Location
CPhI ISCE 2015
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Immunogenicity assay development for biopharmaceuticals requires a case-by-case approach

Authors
Justine Fourmeau
Pierre Damien Misson
Stéphanie Pennincx
Benjamin Albertani
Céline Hoareau
Vincent Van Mullem
Location
EBF Focus meeting 2011
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Combination of GC, UPLC, CE and MS for the characterization of monoclonal antibody glycosylation

Authors
Arnaud Delobel
Géry Van Vyncht
Location
Bioprocess International 2010
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Webinar

Excipient & API suppliers: ICH Q3D is also for you!

Access this 30 minute webinar to learn how the Q3D guideline for EIs can be efficiently implemented for all drug substances, excipients and drug products.
Authors
Philippe De Raeve, Scientific Director
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Elemental Impurities: How to be compliant with Q3D ?

Access this webinar which presented how the Q3D guideline for EIs can be efficiently implemented for all drug substances, excipients and drug products.
Authors
Philippe De Raeve, Scientific Director
Download the slides