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Research supplier
Amatsigroup
Amatsigroup is listed as a mid sized business research supplier in the Scientist.com network, with 2 sites in 2 countries and 2 service areas.
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Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Mid sized business
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.
- 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.
- Excipient Compatibility Test excipients for drug formulation, effects of temperature, time, humidity, pH and light exposure as well as excipient release.
Show all 13 in Chemical and Compound Analysis
- Inductively Coupled Plasma (ICP) Analysis Characterize ultra-small levels of multiple solid analytes simultaneously.
- Particle Size Analysis Measure particle size distribution and characterize particle size, porosity and composition.
- Photostability Measure drug degradation rates after exposure to various light sources.
- Process Residual Impurities Detection Measure trace levels of impurities.
- Solubility Studies Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
- UV-Spectroscopy Conduct sample analysis based on light absorption and transmission.
- Viscosity Testing Evaluate the fluid flow properties of liquids for product evaluation and quality control.
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.
- Bulk Manufacturing Find facilities for large-scale mass production.
- Chemistry Manufacturing Controls Access contract manufacturing and regulatory guidance in setting specifications and drug dosage formulations.
- 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.
- Fill and Finish Processing Confirm final product sterility, formulation and packaging in the biopharmaceutical process.
Show all 11 in Chemistry, Manufacturing and Controls (CMC)
- Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.
- 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.
- Tablet Manufacturing Use automatic or semi-automatic machinery to create various standard and non-standard tablets.
- Thermo Scientific iCAP Q ICP-MS Expand your analytical capabilities with this complete trace elemental analysis solution for your high-throughput lab.
Show all 31 services
Food Safety & Regulations
- Water Activity Determine water activity in consumer healthcare products involving a USP or FCC monograph.
Processing, Packaging, & Preservation
- Liquid Blending Use automatic or semi-automatic liquid blending machinery to produce consistent mixes.
Testing Services
- Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown 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.
Service areas:
Where it operates
Sites by country, with the cities in each.
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Belgium 1 site
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France 1 site
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Amatsigroup offers a wide range of international services in its four strategic business areas: BioseAmatsigroup offers a wide range of international services in its four strategic business areas: Bioservices (in vivo studies & bioanalysis), Pharmaceutical Analysis Solutions, Formulation Development & Manufacturing and also Packaging and Logistics of Clinical Batches. Under GLP & GMP environment (European & US accreditations). Amatsigroup has 5 operational sites in Europe (Amatsi, AmatsiAvepharm, AmatsiAvogadro, AmatsiDBi, AmatsiSEPS) and 1 site in the USA (Amatsigroup Inc.) rvices (in vivo...
Show the full description
Amatsigroup offers a wide range of international services in its four strategic business areas: BioseAmatsigroup offers a wide range of international services in its four strategic business areas: Bioservices (in vivo studies & bioanalysis), Pharmaceutical Analysis Solutions, Formulation Development & Manufacturing and also Packaging and Logistics of Clinical Batches.
Under GLP & GMP environment (European & US accreditations).
Amatsigroup has 5 operational sites in Europe (Amatsi, AmatsiAvepharm, AmatsiAvogadro, AmatsiDBi, AmatsiSEPS) and 1 site in the USA (Amatsigroup Inc.)
rvices (in vivo studies & bioanalysis), Pharmaceutical Analysis Solutions, Formulation Development & Manufacturing and also Packaging and Logistics of Clinical Batches.
Under GLP & GMP environment (European & US accreditations).
- Website
- www.amatsigroup.com
Work with Amatsigroup on Scientist.com
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