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Skyepharma Production S.A.S.
Skyepharma Production S.A.S. is listed as a mid sized business research supplier in the Scientist.com network, with 3 sites in 1 country.
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Sites
3
Countries
1
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
- 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.
- Photostability Measure drug degradation rates after exposure to various light sources.
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 Distribution API and Drug Product Storage and Distribution.
- API and drug product storage and release API and drug product storage and release
- 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 22 in Chemistry, Manufacturing and Controls (CMC)
- 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 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.
- 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.
- ICH-compliant stability testing Perform ICH-compliant stability testing
- 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.
- Raw Materials & Ingredients Purchase raw materials, ingredients, or chemicals for personal care, cosmetic, consumer health, and beauty products and substances.
- Tablet Manufacturing Use automatic or semi-automatic machinery to create various standard and non-standard tablets.
Commercial Consulting
- Production Process Consulting Use expert advice to identify sustainable improvements for manufacturing process operations.
Discovery Chemistry
- Extractable and Leachable Assessment Quantify potential impurities from container closures & packaging.
- Leachable and extractable testing Leachable and extractable testing
Show all 40 services
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.
In Vitro Assays
- Microbiology Study microbes and their role in human health.
Nanotechnology
- Drug Delivery Technology Create microstructures that enhance drug metabolism properties.
Other Specialty Toxicology
- Biosafety Testing In Vitro Test biologics, raw materials, lot release and viral safety
Product Development
- Oral Care - Manufacturing Manufacturing services for oral care products
- Oral Care Products - Formulation Formulation services for oral care products.
- Over-The-Counter (Other) - Manufacturing Other manufacturing services for Over-The-Counter (OTC) products
- Over-The-Counter/OTC (Other) - Formulation Other formulations for Over-The-Counter (OTC) products
Testing Services
- 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.
- Raw Material Microbiological Testing Examples of which include Microbial Content using USP <61> and <62> and other standards, LAL Endotoxin, Ames Mutagenicity and Sterility.
- USP <62> Microbial Limits Test Determine the presence or absence of specific microorganisms.
- Website
- www.skyepharma.com
Where it operates
Sites by country, with the cities in each.
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France 3 sites
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