CDMO Services

Your Full-Service Peptide Partner, Ready When You Are

Supporting your peptide project from discovery, over development, all the way to commercial launch — with available capacity and a proven track record in GMP manufacturing.

Preclinical & Clinical Development

API Manufacturing

Flexible manufacturing solutions, including non-GMP and GMP batches, to support preclinical and clinical development phases.

Process Development

Comprehensive scale-up, process optimization & validation services to ensure robust, reproducible peptide manufacturing processes.

Analytical Development

We offer method development, validation, and stability studies to support product characterization and regulatory readiness.

Regulatory Support

Expert preparation of CMC documentation for clinical Phases 1 to 3, aligned with international regulatory requirements.

Stability Studies

Our team conducts comprehensive long-term and accelerated stability studies to ensure your product’s shelf life during the clinical phase and beyond

Client Project Management

Dedicated project managers ensure transparent communication, clear timelines, and seamless delivery of your project from start to finish.

Commercial Manufacturing

Large-Scale GMP Supply

We offer scalable GMP peptide manufacturing to meet commercial supply needs with unwavering consistency and quality. Our facilities are equipped for high-throughput production while maintaining strict adherence to cGMP guidelines. With free SPPS capacity and robust batch-to-batch reproducibility, we’re ready to support your product launch and beyond.

Filing Support

We provide hands-on support for regulatory submissions, including preparation of technical documentation and response strategies for agency queries. Our experience with global regulatory bodies ensures smoother, faster approval processes for your peptide-based products.