9. What role does 0818 play in the Drug Life Cycle? Select all that apply. a. Provide guidance and regulatory oversight to industry on a wide variety of clinical, scientic, and regulatory matters relating to generic drugs b. Conduct study-directed and comprehensive surveillance inspections of rms that conduct bioavailability/bioequivalence (BA/BE) and Good Laboratory Practice (GLP) studies sometimes with ORA investigators in support of human drug applications. c. Conduct research to expand our knowledge of clinical pharmacology to better evaluate benet and risk d. Protect the public health by applying statistical approaches for monitoring the effectiveness and safety of marketed drugs and therapeutic biologic products