Menovo Pharmaceutical

With 5 cGMP inspected sites and strong R&D (over 100 scientists, state-of-art equipment) we offer CDMO/CMO services for FDFs, APIs and intermediates and customized pharma grade reagents and ingredients. Fast and competitive player, serving EU/US/JP/CN markets. 18 years of compliance track record (no warning letters/recalls) in challenging chemistries (azides, cyanation, nitration, halogenation, high pressure hydrogenation, chiral heterocycles) and oral solid dosage forms (tablets and capsules).