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Filab
Filab is listed as a mid sized business research supplier in the Scientist.com network, with 2 sites in 1 country.
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2
Countries
1
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Mid sized business
Agricultural Sciences Compliance and Quality Control Measures
- Residue Chemistry Pesticide residue and tolerance testing.
Agricultural Sciences Research & Development
- Agrochemical Identification Product identification and composition of pesticides; which includes fungicides, insecticide, herbicides and nematicides analysis.
- Agrochemical Physio-Chemical Testing Conduct extensive property characterization of agrochemicals for geo-specific product approval and registration.
- Chemical and Physical Determination of chemical and physical properties of pesticide product.
- DNA/Protein analysis Analyze DNA and proteins for allergens, pathogens and species identification.
Antibodies
- Antibody Protein De Novo Sequencing Sequence antibody proteins using multiple enzyme digestion and high-resolution LC-MS/MS.
- Antibody Purification Purify multiple antibody types including IgG, IgM, IgA and IgY.
- Epitope Mapping Map the antibody-antigen binding region to define protein-protein interaction sites.
- Immunodetection Use antibodies to identify a protein or antigen.
- Pepscan Analysis Screen overlapping peptide sequences to identify linear epitopes.
Bioimaging
- Confocal/Optical Microscopy Use optical imaging technique to increase optical resolution and contrast of a micrograph.
- Cryo Electron Microscopy Examine the 3D structure of biological complexes and organelles.
- Electron Microscopy Examine the fine structures of molecules, cells and tissues with sub-nanometer resolution.
- Microscopy Use microscopy to analyze surfaces of biological materials and to develop 3D images of biological structures.
- Scanning Electron Microscopy Examine the fine structures of molecules, cells and tissues with sub-nanometer resolution.
- Super Resolution Microscopy Utilize fluorescence microscopy and super-resolution techniques including STED, SIM, SMLM, and/or STORM to directly observe living subcellular structures and activities.
Show all 137 services
Biomarkers
- Biomarker Analytical Validation Assess and optimize the characteristics of a candidate biomarker to ensure reproducibility and consistency.
- Large Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of small molecules.
- Peptide Bioanalysis Analyze the structure of Peptides.
- Protein Bioanalysis Quantitative measurement of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and Proteins in biological systems
Chemical and Compound Analysis
- Accelerator Mass Spectrometry Detect trace levels of naturally-occurring radionuclides and stable nuclides.
- Amino Acid Analysis (AAA) Determine protein quantities, relative compositions and amino acid content profiles.
- Analytical Separations and Purification Analytical Separation and Purification of compound/molecule.
- API Physical Characteristics Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
- Atomic Force Microscopy Use atomic force microscopy to reveal information about the atomic topography and mechanical properties of a sample.
- Centrifugal Precipitation Chromatography Separate analytes based on their solubility in ammonium sulfate solution.
Show all 53 in Chemical and Compound Analysis
- Chiral Separation Purify therapeutically active isomers of drug candidates.
- Circular Dichroism Examine the secondary structure and folding properties of proteins in solution.
- Denaturing High Performance Liquid Chromatography Separate mixtures of denatured and reannealed oligos to identify single nucleotide substitutions, deletions and insertions.
- Differential Scanning Calorimetry Elucidate the thermodynamics associated with conformational transitions.
- Dynamic Mechanical Analysis Measure mechanical properties of solids and polymer melts as a function of time, temperature and frequency.
- Electrophoresis Separate nucleic acids or proteins based on physical properties such as charge or mass.
- Elemental Impurity Analysis Identify and evaluate the presence of heavy metals in pharmaceuticals.
- Filler Content Analysis Evaluate filler material to optimize product performance and process conditions.
- Focused Ion Beam Apply a highly focused beam of gallium ions to remove material at high spatial resolution.
- Headspace Gas Chromatography Analyze volatile organic compounds (VOCs) partitioned above the liquid/solid phase of a sample.
- Heavy Metals Analysis Ensure trace levels of heavy metals are below the maximum allowable limits for consumer safety.
- High Resolution MS Elucidate the sequence and structure of peptides, proteins, biomarkers and organic compounds.
- Impurities in API Risk assessment Create a risk-based control strategy to determine any impurities in Active Pharmaceutical Ingredients (API).
- Inductively Coupled Plasma (ICP) Analysis Characterize ultra-small levels of multiple solid analytes simultaneously.
- Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) Analysis Detect metals and several non-metals at concentrations as low as one part in 1015 (part per quadrillion, ppq) on non-interfered low-background isotopes.
- Ion Exchange Chromatography Separate and detect analytes.
- Liquid Chromatography Separate substances using a mobile and stationary phase.
- MALDI-TOF Analysis Use mass spectrometry technique to analyze compound, biomolecules and large organic molecules.
- Nano-High Performance Liquid Chromatography Separate and detect low levels of analytes.
- NMR Methods Use nuclear magnetic resonance spectroscopy to identify drug intermediates.
- NMR Structure Determine molecular structure, identify chemical impurities and validate sample integrity.
- Non GLP Large Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of large biomolecules.
- Non GLP Small Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of small molecules.
- Optical Rotation Distinguish between optical isomers as well as between natural versus man-made compounds.
- Optical Tomographic Imaging Use multiply-scattered light to reconstruct images of illuminated objects.
- Particle Size Analysis Measure particle size distribution and characterize particle size, porosity and composition.
- Physicochemical Analysis Physicochemical Analysis of material or preparation evaluating (e.g.) particle size, composition, or compound structure.
- Process Residual Impurities Detection Measure trace levels of impurities.
- Protein Binding HPLC Uses high pressure liquid chromatography to separate protein-drug complexes.
- Protein Melting Point Analysis Assess protein stability by Differential Scanning Calorimetry (DSC) or Fluorimetry (Thermofluor) methods.
- Protein Separation and Detection Separate proteins based on properties such as solubility, adsorption or size differences.
- Protein Structure Determine the three dimensional structure of a protein by NMR or x-ray crystallography.
- Scanning and Transmission Electron Microscopy Examine the fine structures of molecules, cells and tissues with sub-nanometer resolution.
- Secondary Ion Mass Spectrometry Detect trace level impurities and obtain elemental or molecular chemical data for solid sample surfaces.
- Size Exclusion Chromatography Separate and identify analytes based on their molecular size.
- Small Angle X-Ray Scattering Obtain low-resolution structures of biopolymers in solution using an x-ray beam.
- Solid State Nuclear Magnetic Resonance Identify molecular structure or impurities and assess product integrity of solid samples.
- Solution Nuclear Magnetic Resonance Identify molecular structure or impurities and assess product integrity of solution samples.
- Spray Drying Convert a liquid into a powder by rapidly drying the mixture and removing the moisture component.
- Structural Chemistry Examine the relationship between protein structure and function.
- Structural Elucidation Determine chemical structure of a compound. Characterization techniques include mass spectrometry, infrared spectroscopy and X-ray crystallography.
- Structural Spectroscopy Assess conformational transitions that proteins undergo in response to changes in their environment.
- Structure Determination Determine the three-dimensional structure of proteins in the presence or absence of ligands.
- UV-Spectroscopy Conduct sample analysis based on light absorption and transmission.
- Viscosity Testing Evaluate the fluid flow properties of liquids for product evaluation and quality control.
- X-ray Microscopy and Nanotomography (Nano-CT) Create two- and three-dimensional imaging of objects in real time.
- X-ray Photoelectron Spectroscopy (XPS) Analyze the surface composition and chemistry of ultra-thin layers of a sample.
Chemical and Compound Testing
- Product Testing Ensure product quality standards are met.
Chemistry, Manufacturing and Controls (CMC)
- Analytical Development and Validation Request services related to Analytical Development and Validation
- API/ Excipients Compatibility Studies Delineate real and possible interactions between potential formulation excipients and the API as an important risk reduction exercise early in formulation development.
- API/DP specific test methods API/DP specific test methods (e.g., stability indicating HPLC assay and purity)
- Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services
- Coating Analysis Evaluate the coat properties of pharmaceuticals, polymers and other finished materials.
- Compendial test methods Run Compendial test methods (e.g., KF)
Show all 12 in Chemistry, Manufacturing and Controls (CMC)
- Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
- Impurities in Drugs Risk Assessment Create a risk-based control strategy to determine any toxic elemental impurities that may be present in human medicines.
- ISO Testing Services for Quality Assessments Testing Services follow standards developed by the International Organization for Standardization (ISO), ensuring consistency, accuracy, and international comparability in various industries including manufacturing...
- Polymorph Screening Screen for unwanted API forms resulting from the drug formulation process.
- Thermal Analysis Characterize compounds based on calorimetry and thermodynamic data.
- Thermo Scientific iCAP Q ICP-MS Expand your analytical capabilities with this complete trace elemental analysis solution for your high-throughput lab.
Clinical Trials
- IP Packaging Proper packaging of pharmaceutical products and goods is crucial to ensure the validity and quality of the product being supplied. Proper investigational product packaging is aided by the use of quality...
Discovery Chemistry
- Extractable and Leachable Assessment Quantify potential impurities from container closures & packaging.
- LCMS Analysis Physically separate substances using liquid chromatography and mass spectrometry.
- Leachable and extractable testing Leachable and extractable testing
- Method Development and Validation Develop and validate methods for synthesis and scale up of drug candidates.
- Structure Property Relationship (SPR) Determine the functionality of a compound through the analysis of it's structure.
- Trace Elemental Analysis Identify organic and inorganic elements in foods and dietary supplements at ppm to sub-ppt levels.
Show all 8 in Discovery Chemistry
- USP Testing Analytical Reagents Acquire chemical reagents, solution concentrates and volumetric solutions used to evaluate items in USP testing.
- UV and IR Profiling Analyze the integrity of a compound or large biomolecule.
DNA & RNA
- De Novo Genome Sequencing Determine the DNA sequence of uncharacterized genomes.
- DNA-lipid interaction analysis Investigate cellular dynamics based on changes in fluorescent properties.
Drug Development
- Chemistry, Manufacturing and Controls (CMC) Consulting Consultant services related to the development of pharmaceutical and biopharmaceutical drug products that are consistently effective, safe and high quality for consumers.
- Structural Chemistry Consulting Expert advice to evaluate the functions of specific chemicals based on their constructions and systems.
Food Safety & Regulations
- Carbohydrate Testing Determine the types and concentrations of carbohydrates in foods for nutritional labeling, quality control, and for identifying possible adulteration.
- Phthalates Analysis Determine the absence of phthalates in food and dietary supplements.
In Vitro ADME
- Metabolite Identification Identify drug metabolites that are formed after administration of drug to an animal model or patient.
- Metabolite Quantification Quantify drug metabolites formed after drug administration to an animal model or patient.
- Metabolite Structural Elucidation Use analytical tools to characterize metabolite structure.
In Vitro Assays
- Lipid Detection Use in vitro methods to identify lipid droplets and any associated proteins.
In Vitro Toxicology
- ADCC and CDC Assay Services Measure toxicity of antibodies.
Medical Communications
- Gap Analysis Compare the actual performance of an organization or corporation with potential or desired performance, as ways to effectively analyze resource management or allocation.
- Market & Competitor Analyses Evaluating the current therapeutic landscape, identifying unmet needs, and assessing the scientific positioning and data of competitor products.
- Medical Devices Biological Evaluation Report Audit Conduct a bio-compatibility evaluation of medical devices within the human body.
Nanotechnology
- Metal/Metal Oxide Nanoparticle Synthesis Use nanoparticles for drug and gene delivery, imaging, analyte detection, labeling and DNA structure determination.
Other Specialty Toxicology
- Raw Materials Testing Verify that raw materials are sterile and not contaminated by mycoplasma, virus or other microorganisms.
- Residual DNA Analysis Measure contaminants found in therapeutics like biologicals and biosimilars that are produced in cells.
- United States Pharmacopeia (USP) Testing Use USP standards to ensure quality of pharmaceuticals, supplements and food ingredients.
Primary Market Research
- Packaging Testing (qual/quant) Evaluates visual appeal, usability, and compliance potential of packaging designs. Data supports regulatory submissions and user-centered design.
Product Development
- Personal/Consumer Care Product or Service Request relating to the creation, testing or manufacturing of a personal care/consumer health/cosmetic product, ingredient or raw material.
Protein Sciences
- Carbohydrate Structure Characterization Use analytical tools to elucidate carbohydrate structure and physiochemical properties.
- Host Cell Protein Analysis Measure contamination of biologics with host proteins by using sequencing, chromatography and the LAL test.
- LCMS/MS Analysis Liquid chromatography–mass spectrometry is an analytical chemistry technique that combines the physical separation capabilities of liquid chromatography with the mass analysis capabilities of mass spectrometry.
- Mass Spectrometry-Based Proteomics Detect histone post-translational modifications (hPTMs), histone variants, and interactomes at chromatin regions.
- NMR Determine molecular and protein structure, and validate sample integrity.
- PEG Protein Conjugation Improve the therapeutic or pharmacokinetic properties of a protein by pegylation.
Show all 14 in Protein Sciences
- Phosphorylation Analysis Identify phosphorylation sites in target proteins.
- Protein Binding Determine drug-protein binding interactions
- Protein Identification Uncover or confirm the identity of a protein.
- Protein Interaction Measure the interaction of a protein to other macromolecules or peptide ligands.
- Protein mapping Interrogate the entire sequence of a protein.
- Protein Post-translational Modification Analysis Measure glycosylation, phosphorylation, sulfation, ubiquitination, methylation and acetylation.
- Proteomics Do large-scale experimental analysis of proteins focused on understanding structure and function.
- X-Ray Crystallography Elucidate structures of biological macromolecules such as proteins and nucleic acids.
Raw Materials
- Plasticizers Excipients designed to modify the physical properties of a basic polymer.
Scientific Data Services
- Automated Image Analysis Automated Image Analysis
Testing Services
- Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
- Characteristic Testing Characterization of physical and chemical properties of raw materials
- Elevated Temperature Stability Determine the stability of a product at elevated temperature.
- Package Compatibility Tests Ensure that the consumer product is not adversely affected by the package components and vice versa.
- Real-time Stability Test Assure stability and physical integrity of consumer products in real-time conditions.
Other services
- New Request
- Website
- filab.fr
Where it operates
Sites by country, with the cities in each.
-
France 2 sites
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