Our factsheet gives an overview of Evotec Modena's capabilities. Download it now to discover more.
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Rare Diseases
Bioinformatics supporting Infectious Disease: Creating knowledge for efficient discovery and development of better medicines.
Pathogen functional genomics analyses for unbiased, multidimensional small molecule effect characterisation (RNA-, DNA-seq analyses to characterise pathogen genome and transcriptome)
Genome assembly and annotation with a focus on resistance and virulence (Illumina, ONT, hybrid)
- Short- (SNP, short indels) and long-range (insertion, deletion, inversion, translocation, duplication) variant analysis associated with resistance (Illumina, ONT)
- Bacterial genome wide association study (GWAS)
- Transcriptome analysis (RNAseq) and functional interpretation
- Bacterial population sequencing and variant characterisation (PoolSeq)
- Molecular phylogeny
- Network analysis (enrichment analysis, pathway mapping)
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Anti-Infectives,
Modelling and Simulation
Learn more about fully integrated development at Evotec.
Evotec is a fully-integrated drug discovery and development partner, providing a comprehensive source of high quality scientific solutions with consultant-level expertise to our partners, which includes fully integrated research and development as well as clinical development through to Proof of Concept.
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Clinical Development
Learn more about our activities for Deep Proteomics at Scale to Drive Biomarker Discovery.
To further boost Evotec’s high-throughput proteomics platform we have implemented the Proteograph™ platform from Seer, which enables automated and unbiased nanoparticle based protein enrichment for maximal proteomic insights.
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Proteomics, Metabolomics & Biomarkers
INDiGO is the fastest and most efficient platform to bring a program from candidate selection through IND and beyond.
Once your clinical candidate is selected, this fully-integrated clinical-enabling package provides inter-disciplinary coordination of all aspects of drug development, conducted and managed by a dedicated Evotec team, and usually at a single Evotec site.
Key features:
- Accelerating your drug discovery and research programs through interdisciplinary integration and expert coordination of all activities “under one roof”
- Industry-leading timelines, taking your program from the selection of an optimal clinical candidate to regulatory submission typically in less than 52 weeks
- Expert management by experienced, dedicated project managers and drug development professionals
- Seamless knowledge transfer across disciplines, maximizing the quality and efficiency of the overall development package
- Custom-designed, flexible development plans that allow for real-time adjustments and adaptability to unforeseeable scientific outcomes
- Excellence in project governance, performance review and issue escalation management
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Formulation & CMC,
ADME/DMPK,
IND Enabling Studies/Preclinical Development,
Toxicology & Safety
Download this fact sheet to learn more about cytochrome P450 (CYP) induction including:
- Background information
- Assay details and protocol summary
- Data generated in the CYP induction assay
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ADME/DMPK
Download this fact sheet to learn more about cytochrome P450 (CYP) relative induction score (RIS) including:
- Background information for the CYP induction RIS method
- Assay details and protocol summary for the CYP induction RIS method
- Data generated in the CYP induction RIS assay
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Fact Sheets,
ADME/DMPK
Download this fact sheet to learn more about hepatocyte stability including:
- Background information
- Assay details and protocol summary
- Data generated in the hepatocyte stability assay
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Fact Sheets,
ADME/DMPK
Learn more about the use of transcriptomics in safety prediction including:
- the challenges in translation from animals to humans, and how human cell-based models are now being routinely used in toxicology
- how transcriptomic analysis is showing promise in enhancing safety prediction and providing additional mechanistic information
- an overview of how Cyprotex, and parent company Evotec, are offering a fully customised end-to-end in vitro transcriptomics service using the latest next generation sequencing technology (RNA-seq) and a leading bioinformatics platform
- the use of sophisticated machine learning and artificial intelligence to interpret the large and complex datasets
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Toxicology & Safety
Download this fact sheet to learn more about formulating your way to successful toxicology studies including:
- Early formulation
- Material science - solid development
- DMPK
- In vitro, in vivo, and in silico models
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Tags:
Fact Sheets,
Formulation & CMC,
Toxicology & Safety