Facility and qualification
Legal entity, production address, applicable licence, registration, GMP or quality-system evidence and audit references.
Quality and documentation
Supplement Manufacturing Qualifications and Documents
Understand which facility, product, batch and export documents can be coordinated, and why every document must be matched to the selected legal entity and project.
Product and batch
Ingredient and product specifications, testing plan, finished-product COA, label file and release records as applicable.
Export and commercial
Packing list, commercial invoice, COO, Free Sale documentation and customs support where the selected entity and market allow.
The applicability rule
No certificate logo applies automatically to every product or factory. Before relying on a document, match its legal holder, address, scope, status and validity to the actual manufacturing activity. We identify those relationships in the project documents instead of presenting the network as one undifferentiated factory.
Need this capability for a product?
Send the target market, dosage form, formula or benchmark, expected quantity, packaging and required documents. We will identify the open questions and applicable production route.
Request a project review