This conference is intended to share information among FDA representatives and the QA regulated community. The program will focus on the relationship between the FDA and QA professionals, implementing regulations, guidelines, and practices, with feedback from experts, to suggest methods and opportunities to enhance research professionals’ product development experience. Sessions will highlight areas that present challenges to sites and studies.

“The Hows and Whys of Internal Standards in Bioanalysis”
Presentation by Katherine Yahvah, PhD, and Rachel Walker, RQAP-GLP
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