Good Manufacturing Practice in the Manufacture of Active Ingredients: The Collected Papers Given at a Seminar Held in Liestal/Basle from 18th to 20th June 1980
Secretariat to the Convention for the Mutual Recognition of Inspections in Respect of the Manufacture of Pharmaceutical Products, 1980 - Drug trade - 97 pages
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Chemical synthesis of active ingredients
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acetanilide acetic acetic anhydride acid active ingredients analytical control aotive application assay Basle batch records Binkert biological chemical production chemical synthesis chemistry compounds defined digitalis Digitalis lanata digoxin distillation drug substance economical end product ethanol example excipients extraction Figure final product finished dosage forms finished product glycosides GMP guidelines GMP regulations GMP rules Hoffmann-La Roche important in-process control ingredients and dosage ingredients and excipients ingredients of natural inspection Intercantonal Office intermediate isolation of active isomer key raw materials lanatoside manufacture of active manufacture of dosage manufacture of pharmaceutical manufacturing process mentioned microbiological molecule natural origin NHcoch obtained his Ph.D operations penicillins pharmaceutical pharmaceutical division pharmaceutical products pharmaceutical quality Phenacetin phenol physical polypeptides ppm max purification procedures purification steps purity testing quality assurance quality characteristic quality control quality requirements reaction Rigassi seminar Sisseln solvents structure Swiss Institute synthesis of active Trimethoprim University of Basle valid vitamin