Mike Riley

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pharmaceutical manufacturing custom pharma solutions analytical method development chromatography drug conjugates highly potent apis pegs lipids process development proteolysis targeting chimeras quality compliance regulatory affairs spray drying technology transfer solid form engineering particle engineering amorphous solid dispersion chiral resolution crystallization development enabling formulation particle size modification physicochemical profiling solid form profiling polymorph screening salt screening cocrystal screening structure confirmation controlled substances bitrex biologics tpds expert insights gmp standards flow chemistry multi-step chemistry antibody-drug conjugates lc-ms hplc sfc impurity isolation quantity production process optimization stability testing safety assessment pharmacokinetics control custom synthesis fatty acids drug delivery applications quality assurance process scale-up technology assessment contract development & manufacturing organization cdmo active pharmaceutical ingredients apis complex chemistries oncology treatments drug development regulatory compliance patient safety supply chain optimization continuous manufacturing cocrystal engineering peptide production solid form optimization pharmaceutical industry biotech partnerships innovation corporate responsibility environmental sustainability customer-centric approach strategic manufacturing footprint advanced manufacturing capabilities clinical trials support targeted drug delivery collaborative partnerships complex molecules drug substance characterization scale-up processes agile supply chain ai integration patient outcomes therapeutic classes generics originators pharmaceuticals medical