Hello guys sana ok lng kau​

Asubject in a clinical research trial experiences a serious, unanticipated adverse drug experience. how should the investigator proceed, with respect to the irb, after the discovery of the adverse event occurrence? a. do not report the adverse drug experience to the irb since it is a common adverse experience.b. report the adverse drug experience to the irb only if there are several other occurrences.c. report the adverse drug experience as part of the continuing review report.d. report the adverse drug experience in a timely manner, in keeping with the irb's policies and procedures, using the forms or the mechanism provided by the irb.

If a simple machine reduces the strength of a force, what must be increased?

Question 1 (5 pts): what is the maximum distance for which you can you resolve the two individual headlights of an on-coming truck as two separate lights rather than one if the headlights are separated by 2.00 m and your eye has a diameter of 1.00 centimeter? assume a wavelength of 500 nm.