Custom design
Solid- and solution-phase peptide pathway design for discovery and pre-clinical programs, complete with rapid analytical guidance.
What we deliver
Integrated peptide advisory modeled after world-class builders.
Focused exclusively on peptides, Superieures packages R&D support, process chemistry, GMP manufacturing design, and lifecycle management so your API is ready for any regulatory audience.
GMP design suites
Conceptual pilot-to-commercial layouts and playbooks that inform your manufacturing partners across the globe.
Lifecycle strategy
Tech transfer planning, validation protocols, regulatory documentation, and global supply orchestration across the peptide lifecycle.
Catalog insights
Ready-to-ship reference peptides, building blocks, and tool compounds to accelerate early research or reformulation efforts.
Lifecycle approach
Peptide programs supported from idea to market.
1. Discovery enablement
Rapid peptide design for SAR campaigns, impurities profiling, and early formulation input with direct access to our chemists.
2. Clinical readiness
GMP-grade peptide API planning, DMF/ASMF authoring support, stability study design, and CMC updates tailored to Phase I-III filings.
3. Commercial continuity
Capacity modeling, redundant raw-material sourcing strategies, and lifecycle change control playbooks to sustain long-term supply via your chosen manufacturers.
Quality DNA
Regulatory-grade rigor for every peptide brief.
Superieures follows US cGMP, ICH, and pharmacopoeial expectations. Our QA/QC design teams create digital batch templates, validated analytical roadmaps, and transparent audit trails ready for global authorities.
Global compliance
US FDA, USP, and international expectations guide every advisory engagement.
Robust analytics
UPLC, LC-MS, HRMS, and orthogonal assay frameworks confirm identity, purity, and potency.
Supply resilience
Dual sourcing models and digital inventory tracking reduce risk from raw-material constraints.
Knowledge hub
Peptide resources for visionaries.
We publish briefs on process chemistry, regulatory changes, and advanced conjugation to keep your teams informed as they build with Superieures.
Whitepaper
Scaling solid-phase synthesis without compromising purity.
Download a GMP-minded approach for high-load resins, green solvents, and automated cleavage.
Insight
Peptide-drug conjugates beyond oncology.
How precision peptides unlock targeted delivery in metabolic and inflammatory diseases.
Playbook
Regulatory-ready peptide CMC packages.
Template-driven documentation modeled on EU & US filings for smoother reviews.