Second Call for Speakers & Posters
European Bioanalysis Forum
3rd Focus Meeting – “Hatching”
Emerging Technologies Approaching the
Regulated Bioanalysis Laboratory
Regulated Bioanalysis Laboratory
With
scientific developments and regulatory expectations not always in concert, our
3rd Focus Meeting aims to connect on the potential of a broad array
of new technologies. We will provide a scientific hub for the development of
strategies, which may enable the application of these emerging technologies to
their full potential in regulated bioanalysis.
Each session
intends to have 4 speakers (1 keynote of 30 minutes and 3 contributions of 20
minutes). For details on the goals and objectives of each session, please visit
the conference website at http://bru2012.europeanbioanalysisforum.eu/program
CALL FOR
SPEAKERS
Potential
speakers, please submit the title and abstract of your presentation before 31
March 2012 to conference address: BRU2012@europeanbioanalysisforum.eu, attaching a
filled out oral presentation submission form available on the conference website. Acceptance of
your presentation will be communicated before 15 April 2011.
CALL FOR
POSTERS
There
will be room for approx. 30 posters and in principle all submitted posters will
be accepted. Please submit the title and abstract of your poster before 15 May
2012 to conference address: BRU2012@europeanbioanalysisforum.eu, attaching a
filled out poster presentation submission form available on the conference website. Supported poster format is
portrait (size A0).
CONFERENCE
PROGRAM
Day 1 - 12
June 2012
Morning
plenary sessions: What's new in Sample Enrichment Technology
Session 1 - Miniaturization and/or automation of sample
preparation techniques
This session will focus on recent progress made in automation and/or miniaturization in support of (regulated) bioanalytical sample preparation. This includes but is not limited to liquid handling technologies, micro extraction and chip technologies. The goal of this session is to share and discuss techniques and processes that will facilitate the sample preparation workflow.
This session will focus on recent progress made in automation and/or miniaturization in support of (regulated) bioanalytical sample preparation. This includes but is not limited to liquid handling technologies, micro extraction and chip technologies. The goal of this session is to share and discuss techniques and processes that will facilitate the sample preparation workflow.
Session 2 - How can antibody technology help with sample
enrichment for NCE or peptides quantification?
This session will focus the use of antibody capture techniques used to optimise sample enrichment for Pharmocokinetic and Pharmacodynamic endpoint technologies.
This session will focus the use of antibody capture techniques used to optimise sample enrichment for Pharmocokinetic and Pharmacodynamic endpoint technologies.
Afternoon plenary sessions:
Recent developments in tissue analysis
Session 3 - Tissue analysis (including micro sampling) and
PK/PD
Over the last years, the analytical potential offered by modern MS technology or immunological approaches opened new avenues in the analysis of non standard matrices for PK, TK or PK/PD reasons. In this session we invite scientist to share their experience or observed scientific, analytical or regulatory hurdles when applying these new technologies. Both MS and LBA scientist will be welcomed.
Over the last years, the analytical potential offered by modern MS technology or immunological approaches opened new avenues in the analysis of non standard matrices for PK, TK or PK/PD reasons. In this session we invite scientist to share their experience or observed scientific, analytical or regulatory hurdles when applying these new technologies. Both MS and LBA scientist will be welcomed.
Session 4 - Is Tissue Imaging approaching quantitative
bioanalysis expectations
The goal of this session is to highlight & discuss the advances and current/potential future use of Tissue Imaging approaches as quantitative bioanalytical tools in a regulated environment.
The goal of this session is to highlight & discuss the advances and current/potential future use of Tissue Imaging approaches as quantitative bioanalytical tools in a regulated environment.
Day 2 - 13 June 2012
Morning
breakout sessions: Miniaturization and diversification in LC – MS interfacing
Session 5 - Miniaturization of LC using ‘conventional’
MS Ionization techniques
Advances made in LC miniaturization, such as microbore and capillary LC, CE, and chip techniques, is opening new possibilities for the bioanalytical scientist. Together with these new possibilities come new challenges. In this session, thoughts and experiences with these techniques will be shared with the aim to enhance the toolset in the (regulated) bioanalytical laboratory and improve problem solving capability.
Advances made in LC miniaturization, such as microbore and capillary LC, CE, and chip techniques, is opening new possibilities for the bioanalytical scientist. Together with these new possibilities come new challenges. In this session, thoughts and experiences with these techniques will be shared with the aim to enhance the toolset in the (regulated) bioanalytical laboratory and improve problem solving capability.
Session 6 - Alternative MS-interfaces for quantitative
bioanalysis
The last 5 years may have been one of the most exciting periods for the bioanalytical scientist with (historically less robust) alternative MS-interfaces (to the commonly used ESI and APCI) coming available to their fullest potential for quantitative bioanalysis. In this session, we aim at providing examples of these alternative MS-interfaces and want to stimulate discussions to enhance their application in (regulated) quantitative bioanalysis.
The last 5 years may have been one of the most exciting periods for the bioanalytical scientist with (historically less robust) alternative MS-interfaces (to the commonly used ESI and APCI) coming available to their fullest potential for quantitative bioanalysis. In this session, we aim at providing examples of these alternative MS-interfaces and want to stimulate discussions to enhance their application in (regulated) quantitative bioanalysis.
Morning
Breakout Sessions: Emerging platforms in support of LBA
Session 7 - Recent new technologies – Methodologies
As the industry looks at options beyond traditional single-plate ELISAs to achieve greater dynamic ranges, analyze multiple analytes or exploit new reporting systems; what are the technology options available (e.g. Flow Cytometry, multiplex analysers etc)? The goal of this session is to showcase & discuss the emerging new LBA technologies & novel LBA methodologies for use in a regulated bioanalysis setting.
As the industry looks at options beyond traditional single-plate ELISAs to achieve greater dynamic ranges, analyze multiple analytes or exploit new reporting systems; what are the technology options available (e.g. Flow Cytometry, multiplex analysers etc)? The goal of this session is to showcase & discuss the emerging new LBA technologies & novel LBA methodologies for use in a regulated bioanalysis setting.
Session 8 - Recent new technologies – Applications and
validation approaches
How are methods being validated on new technology platforms? This session aims to identify and discuss best practices for the validation package requirements of novel LBA applications - are these bespoke or can traditional ELISA method validation packages be used?
How are methods being validated on new technology platforms? This session aims to identify and discuss best practices for the validation package requirements of novel LBA applications - are these bespoke or can traditional ELISA method validation packages be used?
Afternoon plenary session:
Global Bioanalysis Consortium Updates
Session 9 - GBC feedback session
Discuss and provide feedback on the progress made in global harmonization of the bioanalysis guidelines (GBC). The intention is to invite 4-5 Harmonization team leads (or a regional representative from those teams) to present the progress of their teams and to engage with delegates for input and feedback.
Discuss and provide feedback on the progress made in global harmonization of the bioanalysis guidelines (GBC). The intention is to invite 4-5 Harmonization team leads (or a regional representative from those teams) to present the progress of their teams and to engage with delegates for input and feedback.
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