blue cross and blue shield of illinois is a health insurance company that provides millions of members across the state of illinois with comprehensive and affordable health plans. the illinois-based company is a licensed affiliate of the blue cross and blue shield association, which operates affiliate organizations in all 50 states. the association is one of the top five organizations who provides millions in contributions to lobby state and federal legislators and senators to enact legislation, which would be favorable for their member companies. in 2014, the association spent $17 million and was active involved in the affordable care act and legislation regarding medicare. the blue cross and blue shield association is engaging in a approach to environmental forces.
(a)- proactive
(b)- inactive
(c)- inactive
(d)- retroactive

Compare and contrast the methods of argument that pertelote and chanticleer use to defend their interpretation of dreams. what is false about each of their arguments?

Astudy that involves interviews of adults is eligible for expedited review. the researcher wants to add an adolescent population (aged 12 to 17) to the study and has designed a parental permission and assent process. no additional changes are planned. which of the following statements about review of the revised protocol is accurate? the research would only be eligible for expedited review if the adolescents are capable of understanding the same consent forms used for the adult population. the research would only be eligible for expedited review if the adolescents have been declared to be emancipated minors. the new research would need full review by a convened irb because children are a protected population. unless the nature of the questions would raise the level of risk to > minimal for adolescents, the research would still qualify for expedited review.

The procedures for reporting potential unanticipated problems involving risk to subjects or others to the irb are: stated in the human subject protection regulations, but not in the drug or device regulationsincluded in the consent processdetermined by research staffdetermined by the institution in its written policies and procedures