Complex peptides are never simple — insoluble sequences, impurity challenges, long development timelines, and regulatory risks can delay programs and impact your drug development program.
Custom Peptide Services
Neuland’s custom peptide synthesis services cover all the pharmaceutical and biotech industry’s peptide requirements. We specialize in the clinical development of simple to complex peptides synthesis and their commercial-scale manufacturing
Custom synthesis, route scouting, process development and validation, and impurity detection to ensure feasibility and optimization.
Comprehensive manufacturing solutions across scale - from clinical trial batches to full- scale commercial production of complex amino acids and FMOC-building blocks
Advanced R&D capabilities, including method validation, impurity profiling, and stability studies, supported by analytical reference standards.
Raw material vendor evaluation and qualification, ensuring seamless scale-up across lab production, pilots, and commercial manufacturing.
CMC preparation and review for peptide APIs, ensuring regulatory compliance with IMPD, IND, NDA, and ANDA registrations
Why partner with us?
- 42+ years of experience– deep chemistry expertise built over decades of solving difficult synthesis and scale-up challenges.
- 2000+ employees driving innovation – a team of scientists, engineers, and regulatory experts dedicated to advancing your peptide program.
- Globally compliant infrastructure – multiple USFDA, EMA, and PMDA-approved facilities with capacity for mg to multi-kg GMP production.
- Speed + Compliance – Integrated services that reduces development timelines while ensuring global regulatory readiness.
- Client-Centric Approach – transparent communication, flexible outsourcing models, and agile partnerships
