We provide non-GMP preclinical sterile manufacturing to generate high-quality material for early development—focusing on pilot batches for stability studies, preclinical batches, and reference material. Using controlled, phase-appropriate sterile handling and defined workflows, we translate your formulation into reproducible batches with consistent critical quality attributes. For preclinical supply, we manufacture batches suitable for PK/PD, efficacy, and toxicology studies, including clear batch documentation, sampling plans, and storage/shipping concepts.
