We design, build, train, and commission end-to-end peptide manufacturing facilities and then support your team for two years after handover to ensure rapid, reliable research and production. Our services combine facility engineering, equipment procurement and installation, regulatory-ready documentation, and hands-on staff training so your lab operates to RUO and cGMP standards from day one.
Manufacturing and process services
- High-purity custom peptide production using optimized solid-phase peptide synthesis (SPPS) workflows engineered for consistent, high-yield output.
- Complex chemistries and peptide engineering: disulfide bond formation, PEGylation, peptide cyclization, non‑standard amino acids, and post‑synthetic conjugations.
- Flexible production modes covering high-throughput combinatorial libraries, lead‑optimization batches, bulk scale-up for preclinical/clinical supply, and private‑label contract manufacturing.
Quality, analytics and downstream processing
- Comprehensive QC and release testing: preparative and analytical HPLC, LC‑MS/MS mass confirmation, purity profiling, endpoint and in‑process analytics.
- Downstream services: TFA removal, desalting, buffer exchange, sterile filtration where required, and lyophilized (vial and bulk) formulations with customized excipient matrices.
- Strong quality management support: SOP development, batch records, deviation handling, CAPA, and assistance preparing for audits and regulatory submissions.
Technology transfer, validation and training
- Full tech‑transfer and scale‑up support: process characterization, method transfer, and reproducibility studies to meet your project milestones.
- Equipment qualification and facility validation: IQ/OQ/PQ protocols, environmental monitoring programs, and utilities design support (cleanrooms, HVAC, GMP water systems).
- Workforce enablement: role‑based hands‑on training programs, competency assessments, operator SOPs, and ongoing mentoring to embed best practices in SPPS, purification, analytics and GMP operations.
Partnership model
- Two years of continuous post‑design support to optimize processes, troubleshoot production, and improve throughput and yield.
- Tailored CDMO partnership options — from project manufacturing and fill/finish to long‑term supply agreements and private‑label solutions — all aligned to your technical specifications and timelines.
Whether you’re focused on discovery peptides, metabolic signaling molecules, or IVD reagents, we deliver a turnkey facility plus the people, processes and analytical infrastructure to produce reproducible, pharmaceutical‑grade peptides.