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Lucideon

Lucideon is listed as a mid sized business research supplier in the Scientist.com network, with 4 sites in 2 countries.

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

Sites 4

Countries 2

Type of company: Mid sized business

Agricultural Sciences Compliance and Quality Control Measures

Product Properties Determination of physical and chemical properties of product

Agricultural Sciences Research & Development

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.
Method Development & Validation Engineer sensitive and selective methods that meet GLP validation requirements to access different agrochemical properties

Bioimaging

Confocal/Optical Microscopy Use optical imaging technique to increase optical resolution and contrast of a micrograph.
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.
X-Ray Powder Diffraction Structural analysis of crystalline powders via X-rays to detect and quantify polymorphs

Biomarkers

Large Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of small molecules.
Peptide Bioanalysis Analyze the structure of Peptides.
Small Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of small molecules.

Chemical and Compound Analysis

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.
Dissolution Profiling Measure release of API from formulation (tablet or capsules) under GMP guidelines.
Dynamic Light Scattering Determine the size of particles and extent of molecular aggregation in a suspension.
Elemental Impurity Analysis Identify and evaluate the presence of heavy metals in pharmaceuticals.

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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
Energy Dispersive X-ray Spectroscopy Identify and estimate the elemental composition of a sample based on x-ray emission patterns.
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
GLP Large Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of large biomolecules.
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.
Impurities in API Risk assessment Create a risk-based control strategy to determine any impurities in Active Pharmaceutical Ingredients (API).
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.
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.
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.
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.
Sample Bioanalysis Determination of concentration of an analyte in biological sample.
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.
Solubility Studies Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
Spray Drying Convert a liquid into a powder by rapidly drying the mixture and removing the moisture component.
Total Internal Reflection Fluorescence Microscopy Visualize single molecule fluorescence at a surface to produce high quality images with low background.
Total Reflections X-Ray Fluorescence Analyze liquid or smooth solid surfaces to detect ultra-trace levels of particles, residues and impurities.
Viscosity Testing Evaluate the fluid flow properties of liquids for product evaluation and quality control.
X-Ray Fluorescence (XRF) Identify and quantify the elemental composition of solid and liquid samples.

Show all 122 services 105 more

Chemical and Compound Testing

Bacterial Water Analysis Analyzing water samples to identify the bacteria present.
USP <2022> Microbiological Procedures for Absence of Specified Microorganisms Determine the absence of objectionable organisms in nutritional supplements.
USP <85> Bacterial Endotoxin Test Test to detect or quantify bacterial endotoxins that may be present in or on a sample.

Chemistry, Manufacturing and Controls (CMC)

Analytical Development and Validation Request services related to Analytical Development and Validation
API manufacturing process development, tech transfer and validation API manufacturing process development, tech transfer and validation
Coating Analysis Evaluate the coat properties of pharmaceuticals, polymers and other finished materials.
Drug Product Stability Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
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.

Show all 10 in Chemistry, Manufacturing and Controls (CMC) 4 more

Formulation Services Assistance when determining the look, texture, fragrance of a product with compatibility with product packaging, knowledge of competitive performance traits and product shelf life.
Impurities in Drugs Risk Assessment Create a risk-based control strategy to determine any toxic elemental impurities that may be present in human medicines.
Milling, grinding, spray-drying Milling, grinding, spray-drying
Thermal Analysis Characterize compounds based on calorimetry and thermodynamic data.

Clinical Consulting

Bioanalysis Consulting Expert advice to properly and effectively discover, evaluate, and measure chemical or biological materials.

Clinical Trials

Protocol Optimization via AI/ML Using of artificial intelligence and machine learning techniques to enhance and streamline experimental protocols or operational procedures for improved efficiency, accuracy, and outcomes.

Data Science/Bioinformatics

Clinical Data Science and Modeling A process that helps make sense of your clinical data
Discovery Data Science and Modeling A process that helps make sense of your discovery data
Discovery Machine Learning/AI Complex analytical approaches to find patterns and make predictions in drug discovery projects.
Translational Machine Learning/AI Complex analytical approaches to find patterns and make predictions in drug discovery projects.

Discovery Chemistry

Bioanalytical Lab Services Bioanalytical Lab Services
LCMS Analysis Physically separate substances using liquid chromatography and mass spectrometry.
Leaching and Aged Leaching Assess the leaching potential of products with studies that follow the formation and movement of metabolites or show restricted leaching under simulated use conditions.
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.

Drug Development

Assay Development Consulting Request consultant services measuring the activity of a drug or biochemical in an organism or organic sample.
Consulting Services Work with consultants who provide expert advice in various areas of research and technology.
Small Molecule Drug Development Consulting Request consulting services related to small molecule development.

Farm & Livestock Solutions

Food Pathogen Testing of Listeria, salmonella, campylab, 0157E coli.

Food Safety & Regulations

E.coli 0157 Tests Isolate and identify the presence of a distinct variant of the E.coli species or its potent toxin in food, water or contact-surface samples.
Listeria spp. Testing Use molecular, immunological or cultured methods to identify potential growth sites for all species of the Listeria genus.
Phthalates Analysis Determine the absence of phthalates in food and dietary supplements.
Pseudomonas spp. Testing Detect the presence and abundance of various cold-tolerant Pseudomonas species that cause or contribute to spoilage in meat, poultry, seafood, dairy or beverages.
Salmonella spp. Testing Use molecular, immunological or cultured methods to identify the presence of Salmonella species in food or contact-surface samples.
Total Viable Count (TVC) Estimate the total living microbial populations present in a food or beverage sample to guarantee product quality.

In Vitro Assays

Assay Development Construct or create new assays or modify existing ones.
In Vitro SPF (Sun Protection Factor) Testing Use in vitro test methods to measure the UVA protection performance of sun protection products.

In Vitro Toxicology

Cytotoxicity Test for effects on cell viability and proliferation

Other Specialty Toxicology

Microbial Testing Test samples for microorganisms, identify species, do bioburden analysis and measure endotoxin levels (LAL).

Processing, Packaging, & Preservation

Preservation and Antioxidant Testing Ensure the foods or dietary supplements are free of preservatives and antioxidants at a potentially harmful level.

Product Development

Brows/Lashes - Formulation Formulation services for brow/lash products
Makeup Removers - Formulation Formulation services for make-up removers
Men's Products - Formulation Formulation for male oriented products.
Oral Care Products - Formulation Formulation services for oral care products.
Over-The-Counter/OTC (Other) - Formulation Other formulations for Over-The-Counter (OTC) products
Personal Care Product Development Services including the formulation, manufacturing, or designing of a personal/consumer care product or packaging.

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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.
Specialty (Other) - Formulation Other formulations for specialty products in personal care

Protein Sciences

Analytical Ultracentrifugation Characterize the interactions and properties of macromolecules in solution.

Raw Materials

Film Formers Develop products that produce a continuous film on surfaces.

Scientific Data Services

Automated Image Analysis Automated Image Analysis
Machine Learning/ AI Predict and model an outcome (e.g. disease progression) based on input variables (i.e. features.)
Scientific Data Visualization Exploration and reporting of data by means of graphs and plots.

Testing Services

Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
ASTM E2315: Time-Kill Procedure (Antimicrobial Testing Study) Assessment of Antimicrobial Activity Using a Time-Kill Procedure
Bacterial Identification Testing Use biochemical and molecular methods to identify unknown microorganisms.
Characteristic Testing Characterization of physical and chemical properties of raw materials
CLSI M26-A: Minimum Bactericidal Concentration (MBC) Determine the lowest concentration of an antimicrobial agent that is lethal to the target bacteria in vitro.
Consumer Care Testing and Substantiation Test personal care products using analytical, in vitro, and microbial test services

Show all 25 in Testing Services 19 more

Cosmetic Preservative Efficacy Test Assess the efficacy of a product's preservative system.
Cosmetics Aerobic Plate Count Determine the level of aerobic bacteria present in a cosmetic or personal care product.
Cosmetics Anaerobic Plate Count Determine the level of anaerobic bacteria present in a cosmetic or personal care product.
Cosmetics Yeast and Mold Count Determine the presence of fungi in a cosmetic or personal care product.
Elevated Temperature Stability Determine the stability of a product at elevated temperature.
Freeze-Thaw Testing Use freeze-thaw cycling to measure the long-term durability of cosumer products.
In Vitro Claim Substantiation Evaluation using FDA Broad Spectrum and/ or ISO 24443
In Vitro Oral Care Product Testing Perform in vitro oral care product testing of dental products to evaluate safety and performance, including assessment for cleaning, brushing, whitening, stain removal, erosion, abrasivity and sensitivity.
In Vitro Skin Models Measure skin model penetration and invasion, photosensitivity and toxicity.
In Vitro Toxicology Testing Non-animal testing employing US and international methodologies for determining irritation and other undesirable potentials.
ISO 11930: Preservative Test Evaluate the antimicrobial stabilization of a cosmetic product as per ISO 11930.
Microbiological Sterility Testing Test the presence of viable microorganisms.
Package Compatibility Tests Ensure that the consumer product is not adversely affected by the package components and vice versa.
PAO Stability Trial Assess the stability of a consumer product under certain storage conditions.
Raw Material Microbiological Testing Examples of which include Microbial Content using USP <61> and <62> and other standards, LAL Endotoxin, Ames Mutagenicity and Sterility.
Real-time Stability Test Assure stability and physical integrity of consumer products in real-time conditions.
USP 51 Cosmetic Preservative Efficacy Test Evaluate the antimicrobial stabilization of a cosmetic product as per USP 51.
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.

Website: www.lucideon.com

United States Greenville, Morrisville, Schenectady 3 sites
United Kingdom Stone 1 site

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