Company Overview Press Releases Events Careers Login
Raysun Biopharma
Raysun cleanroom team reviewing sterile manufacturing operations

Development Services

Services OverviewIntegrated pathways for peptide APIs and sterile drug-product development Peptide API DevelopmentProgram planning from API strategy through analytical and process development Sterile FDF DevelopmentFormulation, presentation selection and technology-transfer planning Project InquiryDiscuss technical requirements, development scope and next steps

Manufacturing & Facility

Manufacturing OverviewMulti-product sterile platform under development in Laos Facility DevelopmentCurrent construction, cleanroom and equipment-integration status SustainabilityResponsible design, utilities and safe systems of work Project UpdatesVerified construction and company progress

Sterile Dosage Forms

Dosage Forms OverviewFlexible product-development presentations Single-Chamber CartridgesCartridge filling and assembly pathways Dual-Chamber CartridgesTwo-component cartridge system development Lyophilized VialsVial filling, freeze-drying and capping pathways
Frequently Asked Questions
Questions About our Peptide and Oligonucleotide CDMO Services

Still need help? Send us a note!

For any other questions, please write us at tides@sinopep.com.
WhatsAppWhatsApp QR