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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
Oligonucleotide synthesis and purification equipment in a pharmaceutical cleanroom

OLIGONUCLEOTIDE

Custom Oligo Quotation Request

Share your oligonucleotide sequence, chemistry, scale, purity and testing requirements. Raysun will review your project specifications and coordinate the appropriate development and manufacturing pathway for qualified research and pharmaceutical programs.

Start Your Oligo Request

CUSTOM OLIGO REQUEST

Oligo Synthesis Quotation Request

Tell us about your oligonucleotide project. Provide the sequence, chemistry, quantity, purity and testing requirements available at this stage.

About Your Project

Please select product grade (research- or GMP-grade):
Is the sequence primarily Phosphodiester, Phosphorothioate, or PMO?
Oligonucleotide Type
Base Type(s)

Additional Details

Additional Testing

About You

Your Address

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Please do not include confidential, patient or sensitive personal information.

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