FAQ-CHU Pharma

FAQ

Disclaimer：All information in FAQ is for business reference only, not medical advice. All specifications shall subject to official COA, SDS and regulatory documents.

Our pharmaceutical raw materials and intermediates meet USP, BP, EP or CP standards according to different items. Batch‑wise COA will be provided for every shipment.

Relevant technical data can be shared with qualified customers upon signing an NDA agreement.

Shelf‑life and storage conditions vary for different products. Please refer to COA or contact our QA department for detailed parameters.

Third‑party testing is acceptable. Testing expenses shall be borne by the buyer, and to be confirmed before order placement.

Yes. Our products are raw materials for pharmaceutical production only. The end‑use shall be determined by buyers.

Strict GMP production process and batch release system are applied. Each batch undergoes full internal testing before release.

We can provide COA, SDS/MSDS, manufacturing license, GMP certificate, Free‑Sale Certificate, TSE‑BSE statement as applicable.

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FAQ

FAQ

1. What pharmacopoeia standards do your products comply with?

2. Could you provide impurity profile, heavy metal and residual solvent data?

3. What are the shelf‑life and storage requirements of your goods?

4. Do you support third‑party laboratory testing before delivery?

5. Are your products only for pharmaceutical manufacturing purpose?

6. How do you control batch‑to‑batch consistency?

7. What kinds of documents can you provide for import registration?