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Eurofins BPT
Eurofins BPT is listed as a large business research supplier in the Scientist.com network, with 13 sites in 7 countries and 2 service areas.
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Sites
13
Countries
7
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Large business
Antibodies
- Immunodetection Use antibodies to identify a protein or antigen.
Biomarkers
- Antimicrobial Effectiveness Testing Measure the efficacy of anti-microbial preservatives added to a product.
Cell Culture and Characterization
- cGMP Cell Banking Request information or a price quote for cGMP Cell Banking services
Chemical and Compound Analysis
- Atomic Absorption Analysis Measure the elemental composition of a diverse array of samples.
- Denaturing High Performance Liquid Chromatography Separate mixtures of denatured and reannealed oligos to identify single nucleotide substitutions, deletions and insertions.
- Elemental Impurity Analysis Identify and evaluate the presence of heavy metals in pharmaceuticals.
- Endotoxin Testing Use standard assays like LAL (Limulus Amebocyte Lysate), rFC (Recombinant Factor C), or MAT (Monocyte Activation Test) to detect and quantify the level of endotoxins in a sample
- Excipient Compatibility Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
- Gas Chromatography Gas chromatography is an analytical technique that separates, identifies, and quantifies compounds in a mixture
Show all 24 in Chemical and Compound Analysis
- 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.
- Immunoaffinity Chromatography Use antibody-antigen interactions to isolate and concentrate analytes.
- 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.
- Melting Point Use melting point analysis to characterize compounds based on calorimetry and thermodynamic data.
- 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.
- Process Residual Impurities Detection Measure trace levels of impurities.
- Protein Separation and Detection Separate proteins based on properties such as solubility, adsorption or size differences.
- Size Exclusion Chromatography Separate and identify analytes based on their molecular size.
- 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.
- Structural Elucidation Determine chemical structure of a compound. Characterization techniques include mass spectrometry, infrared spectroscopy and X-ray crystallography.
Chemistry, Manufacturing and Controls (CMC)
- 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.
- Excipients Acquire synthetic or natural inert components to formulate therapeutic agents.
- Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
- Regulatory Starting Materials Sourcing regulatory starting materials (RSM)
- Thermo Scientific iCAP Q ICP-MS Expand your analytical capabilities with this complete trace elemental analysis solution for your high-throughput lab.
Show all 80 services
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.
- UV and IR Profiling Analyze the integrity of a compound or large biomolecule.
DNA & RNA
- DNA Sequencing Determine the nucleotide sequence of DNA samples.
- Genotyping Examine a DNA sequence to identify specific genetic varients .
- NGS: Next Generation Sequencing Sequence millions of template DNA molecules in parallel.
- qPCR Analysis Measure the accumulation of PCR products in real time.
- RNA Sequencing Use Next Generation Sequencing techniques to Identify RNA transcripts, examine differential expression patterns and analyze splice variants.
- Sanger Sequencing Sequence single strand DNA fragments using DNA Polymerase.
Drug Development
- Pharmacology Consulting Request consulting services related to pharmacology and the chemical properties, biological effects, and therapeutic uses of drugs.
Effectiveness
- Antimicrobial Pharmacodynamics Ascertain the effectiveness of an antimicrobial compound and test levels of antibiotic resistance against specific bacterial pathogens.
In Vitro ADME
- Reference Standards Find reference standards for assays, tests and services.
In Vitro Assays
- Assay Development Construct or create new assays or modify existing ones.
- Cell Based Assays Apply compounds to cells and test for cellular phenotypes and effects on gene expression
- Endpoint Dilution Assay (TCID50) Assay Determine the viral titer to induce cell death in half the cell population of an inoculated tissue culture.
- Lipid Detection Use in vitro methods to identify lipid droplets and any associated proteins.
- Microbiology Study microbes and their role in human health.
- Reactive Species Assays Use biochemical, cell-based or in vivo assays to detect and evaluate the effects of reactive species.
Show all 8 in In Vitro Assays
- Viral Clearance Assays Measure the capacity to remove or inactivate infectious agents during the manufacturing process.
- Virus Detection Assays Use ultra-sensitve methods to reliably detect low level viruses.
In Vitro Pharmacology
- Drug Target Assays Gain insight into the selectivity and mode-of-action of a compound's pharmacological targets.
- G-Protein Coupled Receptor (GPCR) Assays Detect ligand binding, receptor dimerization and downstream signal transduction events.
- Immuno-oncology Assays Use biochemical, cell based or in vivo assays to measure the activity of immuno-therapy targets.
- Immuno-oncology Targets Develop drugs that take advantage of the immune system to target cancer cells.
- Programmed Cell Death-1 (PD-1) Assays Use biochemical, cell based or in vivo assays to measure PD-1 receptor activity.
- Ubiquitin Ligase Assays Measure ligase enzyme activity in the presence of cofactors or chemical modifiers.
Show all 7 in In Vitro Pharmacology
- Vascular Endothelial Growth Factor (VEGF) Assays Use biochemical, cell based or in vivo assays to monitor competitive or non-competitive binding of VEGF ligand.
In Vitro Toxicology
- ADCC and CDC Assay Services Measure toxicity of antibodies.
Lab Supplies, Facilities, and Equipment
- Biobanking Store and track biological samples.
Other Specialty Toxicology
- Biosafety Testing In Vitro Test biologics, raw materials, lot release and viral safety
- Raw Materials Testing Verify that raw materials are sterile and not contaminated by mycoplasma, virus or other microorganisms.
- United States Pharmacopeia (USP) Testing Use USP standards to ensure quality of pharmaceuticals, supplements and food ingredients.
- Viral Testing Characterize viral products for functional activity and possible contamination.
Product Orders
- Kits and Reagents Submit a request to multiple vendors for kits and reagents.
Protein Sciences
- 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.
- Protein Binding Determine drug-protein binding interactions
- Protein Products Find native and recombinant proteins and peptides.
Raw Materials
- Cationics Positively charged surfactant molecules.
- Drug Actives (Other) Formulate and develop products that contain active ingredients such as salicylic acid, benzoyl peroxide, azelaic acid, tacrolimus, and pimecrolimus.
- Non-Surfactant Modify the interface between solid particles and the liquid medium to improve the particles' resistance to settling.
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
- Raw Material Microbiological Testing Examples of which include Microbial Content using USP <61> and <62> and other standards, LAL Endotoxin, Ames Mutagenicity and Sterility.
- USP <61> Microbial Limits Test Determine whether a substance or preparation complies with an established specification for microbiological quality.
- USP <62> Microbial Limits Test Determine the presence or absence of specific microorganisms.
Other services
- New Request
Service areas:
Biology
Chemistry
Where it operates
Sites by country, with the cities in each.
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France 6 sites
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Netherlands 2 sites
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Germany 1 site
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Hungary 1 site
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Ireland 1 site
Showing 5 of 7 countries.
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Provider of comprehensive laboratory services in the pharmaceutical and biopharmaceutical sciences • Complete CMC Testing Services - all starting material, intermediates, drug substance, drug product, and manufacturing support • Broad Technical Expertise - Chemistry, Biochemistry, Molecular & Cell Biology, Virology, and Microbiology • Full Service Capabilities - Stability, Release, Method Development and Validation • Flexible Service Model options include Fee for Service, Full Time Equivalents (FTE) and Professional Scientific Staffing (PSS) • cGMP compliant, state-of-the-art facilities...
Show the full description
Provider of comprehensive laboratory services in the pharmaceutical and biopharmaceutical sciences
• Complete CMC Testing Services - all starting material, intermediates, drug substance, drug product, and manufacturing support
• Broad Technical Expertise - Chemistry, Biochemistry, Molecular & Cell Biology, Virology, and Microbiology
• Full Service Capabilities - Stability, Release, Method Development and Validation
• Flexible Service Model options include Fee for Service, Full Time Equivalents (FTE) and Professional Scientific Staffing (PSS)
• cGMP compliant, state-of-the-art facilities in the US and Europe
- Professional associations
- AAPS
- Website
- www.eurofins.com/biopharma-services/product-testing
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