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Excite Pharma Services
Excite Pharma Services is listed as a small business research supplier in the Scientist.com network, with 2 sites in 1 country.
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Sites
2
Countries
1
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Chemical and Compound Analysis
- Chemical Stability Measure the stability of small molecules in solution.
- Chiral Separation Purify therapeutically active isomers of drug candidates.
- Dissolution Profiling Measure release of API from formulation (tablet or capsules) under GMP guidelines.
- Excipient Compatibility Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
- Filler Content Analysis Evaluate filler material to optimize product performance and process conditions.
- GLP Large Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of large biomolecules.
Show all 20 in Chemical and Compound Analysis
- GLP Small Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of small molecules.
- 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.
- 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.
- Melting Point Use melting point analysis to characterize compounds based on calorimetry and thermodynamic data.
- 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.
- Partition Coefficient Determine lipophilicity (hydrophobicity) of compounds by measuring log P.
- Photostability Measure drug degradation rates after exposure to various light sources.
- Secondary Ion Mass Spectrometry Detect trace level impurities and obtain elemental or molecular chemical data for solid sample surfaces.
- Solubility Studies Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
- Viscosity Testing Evaluate the fluid flow properties of liquids for product evaluation and quality control.
Chemistry, Manufacturing and Controls (CMC)
- Bulk Raw Materials Acquire raw materials in large volumes at wholesale pricing.
- Chemistry Manufacturing Controls Access contract manufacturing and regulatory guidance in setting specifications and drug dosage formulations.
- Coating Analysis Evaluate the coat properties of pharmaceuticals, polymers and other finished materials.
- Drug Formulation Combine substances including the active drug into a final product with the desired metabolic and therapeutic properties.
- Drug Product Stability Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
- Emulsifiers & Solubilizers Acquire emulsifiers and solubilizers to use as ingredients in consumer healthcare products.
Show all 17 in Chemistry, Manufacturing and Controls (CMC)
- 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.
- Oxidizers/Bleaches Acquire oxidizers/bleaches, such as hydrogen peroxide and sodium hypochlorite, to use as ingredients in consumer healthcare products.
- Phosphates Acquire phosphates to use as ingredients in consumer healthcare products.
- Plant Extracts Acquire plant extracts, such as lutein, lycopene, and quinine, to use as ingredients in consumer healthcare products.
- Polymorph Screening Screen for unwanted API forms resulting from the drug formulation process.
- Powder Blending Use automatic or semi-automatic powder blending machinery to produce consistent mixes.
- Powder Filling Use manual, automatic or semi-automatic machinery to package a variety of powder and granules.
- Product Insert Packaging Use product insert or leaflets to inform patients, satisfy regulatory requirements or extend a coupon offer.
- Salt Form Selection Use high-throughput automated arrays to combine APIs with multiple salts and ions to optimize formulation.
Show all 61 services
Discovery Chemistry
- Certified Standards Find certified standards for assays, tests and services.
- Extractable and Leachable Assessment Quantify potential impurities from container closures & packaging.
- Impurity Synthesis Use high resolution MS or NMR to eliminate intermediates or organic byproducts and determine impurity content.
- Method Development and Validation Develop and validate methods for synthesis and scale up of drug candidates.
- Polyethylene Glycols (PEGS) Acquire polyethylene glycols (PEGS) to use as ingredients in consumer healthcare products.
- Trace Elemental Analysis Identify organic and inorganic elements in foods and dietary supplements at ppm to sub-ppt levels.
Show all 9 in Discovery Chemistry
- USP Testing Analytical Reagents Acquire chemical reagents, solution concentrates and volumetric solutions used to evaluate items in USP testing.
- USP-NF Grade Chemicals Acquire chemicals that comply with United States Pharmacopeia and National Formulary standards.
- UV and IR Profiling Analyze the integrity of a compound or large biomolecule.
Food Safety & Regulations
- Methylmercury Analysis Ensure methylmercury concentration in products is below the maximum allowable limits for consumer safety.
- Phthalates Analysis Determine the absence of phthalates in food and dietary supplements.
New Product Development
- Vitamins Analysis Analyze vitamins in foods and dietary supplements either by HPLC or titration.
Processing, Packaging, & Preservation
- Liquid Blending Use automatic or semi-automatic liquid blending machinery to produce consistent mixes.
Product Development
- Dietary Supplement Manufacturing Prepare standardized and quality nutraceuticals that meet consumer regulatory standards.
Protein Sciences
- Quantitative MS Quantify small and large molecules in the pg/ml range
Raw Materials
- Conditioners & Emollients (Hair & Skin Care) Acquire conditioners and emollients to use as ingredients in consumer healthcare products.
- Surfactants - Amphoterics, Anionics, Betaines, Ethoxylated Glycerine, Nonionics Acquire surfactants, such as amphoterics, anionics, betaines, ethoxylated glycerine, and nonionics, to use as ingredients in consumer healthcare products.
- Vitamins and Derivatives Acquire vitamins and derivatives to use as ingredients in consumer healthcare products.
Testing Services
- Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
- 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.
- 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.
- Real-time Stability Test Assure stability and physical integrity of consumer products in real-time conditions.
- Website
- excitepharma.com
Where it operates
Sites by country, with the cities in each.
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United States 2 sites
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