What Aidacru Supports
Our project work covers gummies, capsules, tablets, powders, softgels, ingestible liquids, drops and pet-supplement formats. Manufacturing feasibility depends on the formula, serving, dosage form, packaging, target market and requested testing or documentation.
| Development | Product brief review, formula direction, ingredient and serving feasibility, flavor or sensory sampling and specification alignment. |
|---|---|
| Manufacturing | Private-label and custom production planning across multiple dosage forms, with the production route confirmed for the actual formula and pack format. |
| Packaging | Bottles, pouches, sachets and other project-specific formats, subject to component availability, artwork approval and line compatibility. |
| Quality documents | Specifications, ingredient information, COA, allergen and non-GMO statements, Supplement Facts support, stability work and third-party reports can be scoped according to the confirmed project. |
How a Project Moves Forward
Define the brief: target country, consumer, formula or ingredient direction, serving, dosage form, claims boundary, packaging and estimated quantity.
Review feasibility: confirm whether the proposed active load, taste, texture and pack count can be manufactured as intended.
Agree the sample plan: define the sample objective, approval criteria and documents needed before commercial production.
Lock the production specification: approve the formula, reference sample, artwork, packaging components and release tests.
Schedule production: the confirmed lead time is based on the active queue, order quantity, raw-material readiness and packaging readiness.
Sampling and MOQ Principles
Aidacru supports both in-stock formula options and custom development. In-stock items may be available from low commercial quantities, while custom MOQ depends on dosage form, pack count, raw-material batch requirements and packaging. Custom sampling often requires an 18-20 calendar-day development-to-dispatch cycle after the project brief is confirmed; this is a planning reference, not a universal guarantee.
Testing and Documentation
The required release and due-diligence package should be agreed for the actual product. Depending on customer requirements, this can include specifications, formula or ingredient information, COA, MSDS, allergen statements, non-GMO statements, Supplement Facts support, stability work and third-party testing.
Third-party laboratory scope, cost and additional timing are confirmed case by case. A raw-material supplier COA, an in-process record and a finished-product third-party report are different documents and should not be presented as interchangeable.
Manufacturing and Certification Transparency
Aidacru coordinates production through a controlled manufacturing operation in Guangdong. Certification documents are available for buyer due diligence and should be reviewed by the issuing body, exact legal certificate holder, facility address, stated scope and validity period.
What to Send for an RFQ
Target country and sales channel
Dosage form and ingredient/formula brief
Amount per serving and servings per container
Flavor, sweetener, dietary and allergen requirements
Packaging type and estimated first order
Required tests, documents and certifications
Artwork status and target launch window
Send the information above so Aidacru can review feasibility, sampling, MOQ, documentation and the next approval milestone. Contact Aidacru.