More Than a CDMO
The End-to-End Support of Your Portfolio
Pre-Clinical
Partner with us for cell line and strain development, manufacturability assessments, cell banking and toxicology material generation. Let us guide your path to IND/IMPD submission.
Clinical Phase I, II
Partner with us to develop your initial clinical process for cGMP drug substance and drug product manufacturing.
Clinical Phase III
Partner with us to optimize, scale and characterize your process to meet anticipated therapeutic demands.
Commercialization
Partner with us for process validation and process performance qualification. Leverage our CMC and regulatory services for your BLA/MAA submission and experience our reliability.
Setting New Standards in
Advanced Therapies and Biologic Advancements
Advanced Therapies
Unlock the future of healthcare with Advanced Therapies – a groundbreaking frontier in medical innovation.
Biologics
Dive into the world of Biologics, harnessing the power of nature for revolutionary medical solutions.