Zasya offers Quick Scale-Up Services are designed to efficiently transition your compounds from laboratory-scale synthesis to larger quantities required for preclinical and clinical development, to both non-GMP and GMP standards.
We conduct thorough assessments of synthetic routes to identify the most efficient and scalable pathways for your compounds.
Utilizing principles of Quality by Design (QbD), we refine processes to enhance yield, purity, and overall robustness.
Execution of non-GMP batches to validate scalability and identify potential challenges prior to GMP production.
Timely provision of high-quality material to support toxicology studies and other preclinical evaluations.
Seamless transition from non-GMP to GMP-compliant processes, ensuring consistency and reliability.
Adherence to cGMP to meet regulatory expectations for clinical trial materials.
Manufacture of clinical trial materials with rigorous quality control to ensure safety and efficacy.
Comprehensive testing and validation to confirm that all materials meet predefined specifications
End to End support
Let’s bring your discoveries to life—faster, smarter, and with unmatched precision with Zasya
