Browse allAgno PharmaCDMO · United StatesFormulation development, analytical development and drug product manufacturing.Request a quoteAsk about this companyWebsite (opens in a new tab)What they doDevelopment & CMCFormulation developmentAnalytical developmentMethod validationParticle engineeringSpray dryingManufacturingDrug product manufacturingLyophilisationAseptic manufacturingFrom their websiteAboutAPI process development (opens in a new tab)Sterile API manufacturing (opens in a new tab)Cgmp injectable finished doseSterile injectable manufacturing (opens in a new tab)Aseptic liquid fill (opens in a new tab)Nanomilling service (opens in a new tab)Complex formulation developmentFeasibility screening (opens in a new tab)GMP clinical materials (opens in a new tab)Nanomilling (opens in a new tab)Hot melt extrusion (opens in a new tab)Micelles (opens in a new tab)Protein assays (opens in a new tab)ELISAs (opens in a new tab)Analytical services capabilitiesMechanical property testing (opens in a new tab)HPLC (opens in a new tab)uPLC (opens in a new tab)GC (opens in a new tab)Dissolution testing (opens in a new tab)Particle size distribution (opens in a new tab)DSC (opens in a new tab)TGA (opens in a new tab)Show all (29)Complex formulation developmentAseptic nanomilling (opens in a new tab)Long-acting dosage forms (opens in a new tab)Controlled release (opens in a new tab)Parenteral formulations (opens in a new tab)ICH stability studies (opens in a new tab)AboutComplex injectables (opens in a new tab)Analytical services capabilitiesComplex dosage forms (opens in a new tab)Cgmp clinicalISO 5 suites (opens in a new tab)Cgmp injectable finished doseSterile CTM formats (opens in a new tab)Quality & certificationsUS FDA inspections (opens in a new tab)GMP (opens in a new tab)ISO 13485 (opens in a new tab)