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Ceutical Laboratories
Ceutical Laboratories is listed as a small business research supplier in the Scientist.com network, with 1 site in 1 country and 3 service areas.
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Sites
1
Countries
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Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Agricultural Sciences Compliance and Quality Control Measures
- Environmental Impact Tests designed to determine environmental impact of product.
- Microbial Pesticides Testing requirements for registration of microbial pesticide products.
- Product Properties Determination of physical and chemical properties of product
- Production and Preservation Assistance with the transfer of primary products to end consumer.
- Residue Chemistry Pesticide residue and tolerance testing.
Animal Science and Welfare Audits
- Vendor Audits/Qualifications vendor audits for non-GLP and GLP nonclinical CROs throughout the US and Canada.
Chemical and Compound Analysis
- Amino Acid Analysis (AAA) Determine protein quantities, relative compositions and amino acid content profiles.
- Atomic Absorption Analysis Measure the elemental composition of a diverse array of samples.
- Chiral Separation Purify therapeutically active isomers of drug candidates.
- 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.
Show all 14 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.
- Inductively Coupled Plasma (ICP) Analysis Characterize ultra-small levels of multiple solid analytes simultaneously.
- 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.
- Optical Rotation Distinguish between optical isomers as well as between natural versus man-made compounds.
- 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 76 services
Chemical and Compound Testing
- Product Testing Ensure product quality standards are met.
- USP <2021> Microbial Enumeration Tests Estimate the total aerobic microbial count, total combined yeast and mold counts, and the presence of bile-tolerant gram-negative bacteria present in nutritional supplements.
- 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 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 Stress Testing Studies Develop analytical methods to predict stability problems and identify degradation products/pathways under forced degradation conditions.
- API/DP specific test methods API/DP specific test methods (e.g., stability indicating HPLC assay and purity)
Show all 15 in Chemistry, Manufacturing and Controls (CMC)
- Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services
- 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.
- Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
- ICH-compliant stability testing Perform ICH-compliant stability testing
- 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...
- Product Insert Packaging Use product insert or leaflets to inform patients, satisfy regulatory requirements or extend a coupon offer.
Clinical Consulting
- Data & Risk Management Determine the extent of the risk and the reliability of the data used to access the aforementioned risk.
- IND Writing Consulting Consulting for an Investigational New Drug Application
- Product Testing Consulting Expert advice to evaluate the effectiveness, quality, and legitimacy of a given item or good.
- Regulatory Compliance & Documentation Regulatory compliance describes the goal that organizations aspire to achieve in their efforts to ensure that they are aware of and take steps to comply with relevant laws, policies, and regulations.
Clinical Trials
- Regulatory Affairs Consulting Receive assistance ensuring compliance with regulatory requirements.
- Regulatory Operations Ensure that all specific regulatory documents are published and properly organized before submission.
Discovery Chemistry
- Compound Synthesis Synthesize small molecule candidates for use in hit followup, lead optimization and medicinal chemistry.
- Custom Synthesis Find or synthesize mg to kg amounts of target-specific and target agnostic compounds for HTS and biological screening.
- 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
- 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.
- Consulting Services Work with consultants who provide expert advice in various areas of research and technology.
- Laboratory Operations Consulting Request consulting services through the Genius Consulting Network™, Scientist.com provides your organization with immediate access to expert consultants with the experience and leadership skills to drive complex...
Food Safety & Regulations
- Anaerobic Plate Count Determine the total anaerobic bacteria present in a food or contact-surface sample.
- Carbohydrate Testing Determine the types and concentrations of carbohydrates in foods for nutritional labeling, quality control, and for identifying possible adulteration.
- Clostridium perfringens Tests Ensure food and water safety by detecting the presence of C. perfringens, its spores or the toxins in samples.
- 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.
- E.coli spp. Testing Use molecular, immunological or cultured methods to detect the presence of E.Coli species in samplings from food, water, contact surfaces or another source.
- Listeria monocytogenes Tests Assess product samples or the direct contact surfaces for a specific and prevalent Listeria species capable of growth at low temperatures.
Show all 13 in Food Safety & Regulations
- Listeria spp. Testing Use molecular, immunological or cultured methods to identify potential growth sites for all species of the Listeria genus.
- Pseudomonas aeruginosa Testing Use molecular, immunological or cultured methods to confirm the presence or absence of P.aeruginosa in samples from food, water or processing surfaces.
- 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.
- Shigella spp. Testing Use molecular, immunological or cultured methods to detect various species of Shigella in food samples.
- Total Coliform Testing Measure the bacterial content of a sample to assess food safety, efficacy of sanitation methods or handling practices.
- 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.
Medical Communications
- Quality Control/ Quality Assurance Documents Develop quality control or quality assurance documents.
Other Specialty Toxicology
- Microbial Testing Test samples for microorganisms, identify species, do bioburden analysis and measure endotoxin levels (LAL).
Pharmacovigilance
- GxP Compliance Monitoring Ensure products or services adhere to a set minimum standard.
Testing Services
- Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.
- Cosmetics safety assessments Conduct safety assessments such as Microbiological quality, Margin of Safety, and information about the packaging material of cosmetic products.
- Freeze-Thaw Testing Use freeze-thaw cycling to measure the long-term durability of cosumer products.
- Microbiological Sterility Testing Test the presence of viable microorganisms.
- Real-time Stability Test Assure stability and physical integrity of consumer products in real-time conditions.
- USP <61> Microbial Limits Test Determine whether a substance or preparation complies with an established specification for microbiological quality.
Show all 7 in Testing Services
- USP <62> Microbial Limits Test Determine the presence or absence of specific microorganisms.
Service areas:
Chemistry
Pharmacology
Toxicology
Where it operates
Sites by country, with the cities in each.
-
United States 1 site
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Ceutical Laboratories offers discovery support, pharmaceutical analysis, clinical manufacturing, APIs, chromtography, and regulatory affairs.
- Website
- www.ceuticallabs.com
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