Scientific Library: results

Publications & Application notes

Alternative analytical solutions for endotoxin and pyrogen testing

Authors
Sara Hully
Paula Paci
Fabian Vandermeers
Géry Van Vyncht
Arnaud Delobel
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Validation of a Monocyte Activation Test (MAT) using the PyroMAT™ kit

Authors
Sara Hully
Fabian Vandermeers
Vincent Bertholet
Géry Van Vyncht
Arnaud Delobel
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Development of orthogonal chromatographic methods for the purity analysis of therapeutic oligonucleotides

Authors
Arnaud Delobel
Claire Butré
Morgane Lescut
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Absolute Quantification of Oligonucleotides by ICP-MS/MS

Authors
Arnaud Delobel
Juliusz Bianga
Magali Perez
Damien Mouvet
Caroline Cajot
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Conference

TIDES Europe Damien Mouvet Oligos ICP-MS

ICP MS/MS: An innovative approach for the characterisation of therapeutic oligonucleotides

ICP-MS/MS: An Innovative Approach for the Characterisation of Therapeutic Oligonucleotides


ICP-MS/MS methodologies were developed for the characterisation of therapeutic oligonucleotides:

Authors
Damien Mouvet
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Oligonucleotide

Characterisation of therapeutic oligonucleotides by ICP-MS/MS

Quality Assistance developed an innovative method for the absolute quantification of therapeutic oligonucleotides, as well as for the determination of phosphodiester-to-phosphorothioate (PO/PS) ratio by ICP-MS.MS.

Authors
Juliusz Bianga
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Quality Assistance Oligonucleotide

Oligonucleotides : absolute quantification and P=O/P=S ratio in a single ICP-MS/MS run

ICP-MS can be a solution for a fast and accurate generic method for oligonucleotides quantification without the reference oligo !
Authors
Philippe De Raeve, Scientific Director
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Q3D - Elemental Impurities

What implications for APIs & excipients suppliers?
Authors
Philippe De Raeve, Scientific Director
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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
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Scientific poster

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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