RFQ review
Product or sequence, quantity, specification, analytical package, packaging and destination are reviewed together.
Peptide Custom Synthesis & OEM / ODM
Contract manufacturing from technical review to batch documentation and optional finished vial presentation.
CDMO Service Scope
Pharmatide Global provides custom peptide synthesis, purification, analytical release, lyophilisation and OEM/ODM packaging within the capabilities stated on this website. Project feasibility, scale, specification, MOQ and lead time are confirmed after technical review.
Project Process
Feasibility and quotation
The synthesis route, scale, MOQ, documentation and lead time are confirmed in writing.
Synthesis and purification
Solid-phase or solution-phase manufacturing is selected according to the approved project scope.
Analytical release
The agreed RP-HPLC, LC-MS, NMR, bioburden or endotoxin package is completed and documented.
Optional fill and finish
OEM or ODM projects can include freeze-dried vial filling, capping, labelling and finished presentation.
Shipment planning
Packaging, carrier, tracking, documents and estimated transit are confirmed for the destination.
OEM / ODM Freeze-Dried Vial Brief
A useful brief should specify peptide content per vial, vial count, vial and closure requirements, label and carton artwork, document requirements and destination. The buyer approves artwork and destination-specific requirements before production.
RFQ Checklist
- Peptide name or complete amino-acid sequence
- Target quantity and repeat forecast
- Required form and specification
- Analytical methods and batch documents required
- Bulk or freeze-dried vial packaging
- Label and carton artwork for OEM projects
- Destination and buyer-side document requirements
Review manufacturing, quality verification, COA requirements and shipment planning.
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