Peptide CDMO FAQ
Answers about project inputs, OEM and CDMO scope, certification, documents, MOQ and confidentiality.
What information is needed for a peptide CDMO quotation?
Provide the sequence or material identity, modifications, target specification, quantity, intended application, documentation needs, destination market and timing.
Do you support OEM, ODM, CRO and CDMO projects?
Yes. Peptide and lyophilized-powder products can be reviewed under those service models according to feasibility and market requirements.
Are ISO 9001, ISO 22000, HACCP and GMP certifications available?
Hytanbio reports these certifications. Current originals, covered entity, scope and validity can be reviewed during supplier qualification.
Can you provide COA and SDS documents?
Available documents are confirmed for the quoted material and relevant batch. Website content does not replace batch-specific evidence.
What are the MOQ and lead time?
They depend on sequence, modification, specification, scale, packaging and testing. They are confirmed after feasibility review.
Can you sign an NDA?
Confidentiality requirements can be discussed before detailed customer-specific information is exchanged.