QUALITY & DOCUMENTATION

Start with the right questions.

Tell us your intended formulation, destination market and specification. A listing begins the qualification process.

Identity & specification

Chemical name and CAS; salt and polymorph; grade; assay; impurities and particle size.

Batch COA, SDS, manufacturing site, origin, GMP evidence and retest information.

For pellets: drug loading, particle size, release profile, dissolution method and coating integrity.

Destination-specific permissions, DMF or CEP relevance and intellectual-property requirements.

Botanical identity, marker content, allergens, microbiological limits and strain-level probiotic identity.

Quantity, packaging, destination, target lead time and sample requirements. Stock and price require confirmation.