Capable CDMO Catachem is an ISO 13485 certified, FDA-registered CDMO with capabilities in lyophilization, bioprocessing materials, and custom reagent formulations. This suggests opportunities to engage for contract manufacturing of diagnostic reagents, culture media, controls, test kits, and niche bioprocessing products for regulated markets.

Expansion Readiness A forthcoming cGMP buildout in 2026 will expand manufacturing capacity for regulated diagnostics, animal health, and biopharma programs, enabling sales conversations around larger scale production of sterile reagents, vaccines/enzymes, and potential small molecule or API manufacturing post-buildout.

Lyophilization Specialty Catachem supports vial, bulk, and bead lyophilization with scalability up to 240 L per vessel, 0.22 micron filtration, and flexible filling. This positions them as a strong partner for customers seeking improved stability and streamlined operations for lyophilized reagents and biologics.

Industry Fit With a focus on clinical chemistry diagnostics, veterinary pharmaceuticals, and biopharma services, Catachem can target diagnostics manufacturers, veterinary vaccine firms, and biotech companies needing compliant manufacturing of culture media, assay reagents, and custom HPLC/UPLC formulations.

Global Quality Footprint Holding ISO 13485 certification and FDA registration, plus a documented capability stack including sterile reagents, UVC sterilization, and batch production, Catachem offers a quality-conscious partner profile appealing to regulated customers seeking reliability and compliance.