This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical and biotech industries, including drug packaging and delivery components, single-use systems, medical devices, and parenteral drug products. It will focus closely on the keys to satisfying recent revisions to several applicable USP chapters, FDA guidances & other international regulatory requirements for best practices in materials and chemistry characterization for drugs, biologics, delivery systems, and primary & secondary packaging.
Join us Thursday, November 5 at 2:50 p.m., as Sainath shares insights on balancing analytical efficiency with patient safety during his presentation, “A Toxicologist’s Perspective: Reducing Analytical Burden Without Compromising Patient Safety”.
Not registered and interested in attending? Email us at askmed@medinstitute.com for further details and receive 20% off your registration!
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