Clinical Research Fastrack instructor Juanita Rendon is a Regulatory Compliance Associate at the largest international CRO, Synexus. She was recently published in Compliance Today for her article discussing the need for continuing ethical practices in research.
In her article she explains why trials should select the study design that best protects the subjects, obtain independent review approval/oversight before study activities begin, and always follow the Informed Consent process. She also discusses why subject selection must be fair and consistent with the scientific purpose, and why researchers should consistently use ALCOAC (Attributable, Legible, Contemporaneous, Original, Accurate, and Complete) guidelines in documentation.
Clinical Research Fastrack is honored to work with the industry’s content experts as we deliver a valuable bootcamp training experience to our students.