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Pharmaceutical process engineering is the term given to the science involved in the conception, design, construction, and operation of research facilities and manufacturing plants, where they also are involved in the conception, design, scale-up, manufacturing, and labelling and packaging processes in the conversion of chemical and biological materials into valuable pharmaceuticals and pharmaceutical therapies. FDA regulations, validation assurance (VA), quality control, and maintain Good Manufacturing Practices (GMP) compliant facilities have to be implemented. Also, environmental and personal safety should also be maintained more

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