The Application of NMR for Drug Development and Manufacturing in a Good Manufacturing Practice Setting
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At Almac, GMP regulations set by the Pharmaceutical regulatory bodies such as the FDA (Food and Drug Administration) and the MHRA (Medicine and Healthcare products Regulatory Authority) ensure that manufacturing processes and facilities are properly designed, monitored and controlled. The GMP environment guarantees the identity, strength, quality and purity of drug products. In this webinar, technical leader at Almac, Kerry Hughes, will discuss the application of NMR in the GMP setting to ensure continued high-quality performance of drug discovery, drug development and manufacturing workflows. The organization has two Bruker instruments for the whole spectrum of GMP activities, from the early phase of development through to the final commercial product, which could be anything from raw materials through to active pharmaceutical ingredients that are ready for release.