Firalis Molecular Precision
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17, Rue du Fort
68330 Huningue
France
Business Development Manager
About us
Firalis Molecular Precision (FMP) is a fast-growing CRO & CDMO, providing advanced multi-omics solutions and tailored contract research services to the Life Sciences sector.
With headquarters in Huningue, France, and a presence in Cambridge, MA, USA, FMP is renowned for its commitment to innovation and excellence.
Our mission is to empower healthcare professionals, researchers, and biopharmaceutical organizations with the tools and solutions they need to make progress towards better patient care and a more personalized medicine
Business offer
Leveraging cutting-edge technology, FMP offers a comprehensive suite of bioanalytical services encompassing biobanking, multiomics-driven analyses (including genomics, transcriptomics, proteomics, lipidomics, and metabolomics), as well as omic data analysis, assay development, and custom IVD kit manufacturing.
Activities
- Service
- Cardiology
- Oncology
- Nervous Central System
- Immunology
- Inflammation
- Target selection & validation
- Gene / protein discovery
- bioinformatics design
- Expression and pathway analysis of target
- quantification of target
- Assay development in in-vitro & in-vivo models
- Research exploratory companion biomarkers
- Hit discovery
- Screening & Identification
- Therapeutic libraries
- In silico
- In-vivo models
- In-vitro & ex-vivo models
- Indication searching
- Bioinformatics prediction & analysis
- Preclinical biomarkers
- Mechanism/Function
- Mechanism of action
- Safety
- PK/PD features
- Indication Identification
- Exploratory toxicology
- Drug-Target interaction
- Level of response duration
- Specificity
- Surrogate markers
- Research exploratory Companion biomarkers
- Bioinformatics design
- Bioinformatics prediction & analysis
- Animal biomarkers
- Human biomarkers
- Predictive biomarkers
- Treatment efficacy
- Population stratification
- Risk/benefit profile
- Disease progression / follow-up
- Bioproduction
- Pilot Batches
- Tests
- Optimization
- Scale-Up process
- Process optimization & validation
- Quality assurance, quality control & analytical process
- Bioproduction analytical test
- Monitoring
- Characterization
- Batch consistency
- Batch release test
- Quality control test support
- Post-production test
- Real-time stability test
- Clinical trials
- Phase I
- Phase II
- Phase III
- Phase IV
- Clinical biomarkers
- Predictive biomarkers
- Treatment efficacy
- Population stratification
- Risk/benefit profile
- Disease progression / follow-up
- Safety
- PK/PD features
- Surrogate markers
- Disease progression monitoring
- Regulatory filing
- Regulatory Filing
- Post-market surveillance
- Post-Market Surveillance