Active Pharmaceutical Ingredient API Method Development and Validation
FDA GMP Pharmaceutical Laboratory needed for development and validation of a CE-UV/ MS compatible method, for impurities determination (MS only as qualitative tool) in synthetic peptide Active Pharmaceutical Ingredient API. I'm looking for a GMP-laboratory with CE equipment coupled to MS (where MS at least MALDI or Q-TOF, only for qualitative identification of impurities in the API)
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