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Curapath

Curapath is listed as a mid sized business research supplier in the Scientist.com network, with 2 sites in 2 countries.

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Search companies, drugs, suppliers and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

Sites 2
Countries 2

Services

What this research supplier says it provides, as listed in the Scientist.com network.

Type of company: Mid sized business

Biomarkers

  • Cell Viability Measure changes in cell number, cell division, DNA content or a cell metabolism marker such as ATP levels.

Cell Culture and Characterization

  • Adherent Cell Culture Grow monolayers of anchorage-dependent cells.
  • Cell Culture Culture primary or immortalized cell lines.
  • Cell Transfection Produce, package and optimize transfection of your siRNA or DNA construct.

Chemical and Compound Analysis

  • API Physical Characteristics Characterize physical and chemical properties of new drug molecules to develop safe, effective, and stable dosage forms.
  • Chemical Stability Measure the stability of small molecules in solution.
  • Dynamic Light Scattering Determine the size of particles and extent of molecular aggregation in a suspension.
  • Electrophoresis Separate nucleic acids or proteins based on physical properties such as charge or mass.
  • 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
  • Impurities in API Risk assessment Create a risk-based control strategy to determine any impurities in Active Pharmaceutical Ingredients (API).
Show all 17 in Chemical and Compound Analysis 11 more
  • Ion Exchange Chromatography Separate and detect analytes.
  • Liquid Chromatography Separate substances using a mobile and stationary phase.
  • 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.
  • Particle Size Analysis Measure particle size distribution and characterize particle size, porosity and composition.
  • Protein Separation and Detection Separate proteins based on properties such as solubility, adsorption or size differences.
  • Raman Spectroscopy Use spectroscopic technique to observe vibrational, rotational and other low-frequency modes in a system.
  • Size Exclusion Chromatography Separate and identify analytes based on their molecular size.
  • Structural Elucidation Determine chemical structure of a compound. Characterization techniques include mass spectrometry, infrared spectroscopy and X-ray crystallography.
  • Structure Determination Determine the three-dimensional structure of proteins in the presence or absence of ligands.

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 and Drug Product Stability Testing API and Drug Product Stability Testing.
  • API and drug product storage and release API and drug product storage and release
  • API manufacturing process development, tech transfer and validation API manufacturing process development, tech transfer 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)
Show all 20 in Chemistry, Manufacturing and Controls (CMC) 14 more
  • Bulk Manufacturing Find facilities for large-scale mass production.
  • Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services
  • Clinical supply management Clinical supply management
  • Compendial test methods Run Compendial test methods (e.g., KF)
  • Drug Formulation Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
  • Drug product packaging and labeling Drug product packaging and labelling
  • Drug Product Stability Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
  • Drug Substance and Drug Product Characterization and Manufacturing Drug Substance and Drug Product Characterization and Manufacturing.
  • Excipients Acquire synthetic or natural inert components to formulate therapeutic agents.
  • Fill and Finish Processing Confirm final product sterility, formulation and packaging in the biopharmaceutical process.
  • Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
  • GMP Synthesis Synthesize APIs including small molecules, formulations and protein-based drugs under GMP compliance.
  • ICH-compliant stability testing Perform ICH-compliant stability testing
  • Impurities in Drugs Risk Assessment Create a risk-based control strategy to determine any toxic elemental impurities that may be present in human medicines.
Show all 68 services 51 more

Clinical Consulting

  • Regulatory Consulting Ensure that each product or device complies with all FDA rules and regulations.

Discovery Chemistry

  • LCMS Analysis Physically separate substances using liquid chromatography and mass spectrometry.
  • Leachable and extractable testing Leachable and extractable testing
  • Lead Optimization Perform chemical structural changes to improve preclinical drug candidate.
  • Method Development and Validation Develop and validate methods for synthesis and scale up of drug candidates.

DNA & RNA

  • Capillary Electrophoresis Separate ng quantities of DNA to single base resolution.
  • Quantitative RT PCR Use quantitative reverse transcription polymerase chain reaction to measure absolute and relative mRNA abundance.

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.

Human Biological Samples

  • Human Immortalized Cell Culture For requesting human cells Cell Lines typically refer to legacy immortalised cells, that can be cultured and passaged “indefinitely” Primary Cells are cells that have been isolated from fresh tissue (or cultures) that...

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.

Medical Communications

  • Investigational Medicinal Product Dossier (IMPD) and Investigational New Drug (IND) Dossier Develop and submit Investigational Medicinal Product Dossier (IMPD) and Investigational New Drug (IND) Dossier
  • Quality Control/ Quality Assurance Documents Develop quality control or quality assurance documents.

Nanotechnology

  • Custom Nanostructures Fabricate materials in the form of spherical particles, nano-tubes, wires, rods, discs, flakes, prisms or dispersions.
  • Drug Delivery Technology Create microstructures that enhance drug metabolism properties.
  • Liposomes Create artificial spherical vesicles that can be used as a vehicle for administration of drugs.
  • Nanoparticle Conjugation and Functionalization Modify biomolecules to enhance structure and function.
  • Nanoparticle Synthesis Create nano-level structures with unique features.
  • Nanostructured Lipid Carriers Formulate nanostructered lipid carriers used in drug delivery systems.
Show all 7 in Nanotechnology 1 more
  • Silica/Polystyrene/Organic Nanoparticle Synthesis Synthesize nanoparticles with distinctive composition, size, shape and surface chemistry.

Protein Sciences

  • NMR Determine molecular and protein structure, and validate sample integrity.
  • PEG Protein Conjugation Improve the therapeutic or pharmacokinetic properties of a protein by pegylation.
  • Protein Purification Isolate native or recombinant proteins from a sample.
  • Qualitative MS Perform direct identification of molecules based on mass-to-charge ratio and fragmentation patterns.
  • Quantitative MS Quantify small and large molecules in the pg/ml range

Other services

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Website
curapath.com

Source: Scientist.com supplier network

Where it operates

Sites by country, with the cities in each.

  • Spain Paterna 1 site
  • United States Cambridge 1 site

Source: Scientist.com supplier network (site locations)

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Sources: Scientist.com supplier network.

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