For licorice ingredients and extracts, we coordinate the selected product’s quality standards, assay methods and batch information. Intended use, registration documents and supply terms are reviewed for each product and production partner.
Product information supports ingredient selection. Contact us to confirm specifications, intended use and availability.
Human Pharma Portfolio / 3
Applications
For sourcing licorice fluid extract; establish the applicable standard and liquid-supply requirements first.
Highlights
Form focus
Review fluid and solid extracts separately; equal weights do not establish equivalence.
Document focus
Confirm standard edition, assay, solvent, packaging and storage information.
Applications
For sourcing licorice solid extract, reviewing the specification for its form and downstream process.
Highlights
Process focus
Confirm incorporation method, moisture requirements and dissolution or dispersion conditions.
Document focus
Review the adopted standard edition and batch COA; select separately from fluid extract.
Applications
For professional sourcing, reviewing the standard and documents for monoammonium glycyrrhizinate S from the actual supply source.
Highlights
Standard focus
Confirm standard name, edition, assay and identification method.
Supply focus
Review product and supplier documents, batch COA, packaging and storage conditions.
Review documents, samples and supply requirements for the specific product.
Compare available ingredients by content, form and intended use.
Review target specifications, assay methods and customer requirements.
Coordinate available batch documents for the product and production partner.
Arrange sample evaluation around the customer’s formulation and process.
Confirm quantity, packaging, delivery location and timing.
Communicate use conditions and document requirements to the relevant partners.
Review requirements, documents and samples to assess ingredient suitability for your project.
Specify the ingredient, target standard, intended use and destination.
Review available quality documents and coordinate sample evaluation.
Confirm quantity, packaging and delivery for the selected grade and availability.
Share the ingredient, target specification, application, quantity and destination so we can coordinate relevant products and documents.