According to the newly adopted protocols by the Ministry of Health, a pharmaceutical company is permitted to bypass the standard three-phase clinical trial only if the medication in question targets a designated rare disease or has already received full regulatory approval in a recognized partner nation.
Which one of the following logically follows from the Ministry of Health's protocols?
- If a medication neither targets a designated rare disease nor has received full regulatory approval in a recognized partner nation, then the pharmaceutical company is not permitted to bypass the standard three-phase clinical trial.Answer
- BIf a medication targets a designated rare disease or has received full regulatory approval in a recognized partner nation, then the pharmaceutical company is permitted to bypass the standard three-phase clinical trial.
- CIf a pharmaceutical company is not permitted to bypass the standard three-phase clinical trial, it must be the case that the medication neither targets a designated rare disease nor has received full regulatory approval in a recognized partner nation.
- DIf a medication does not target a designated rare disease, or if it lacks full regulatory approval in a recognized partner nation, then the pharmaceutical company is not permitted to bypass the standard three-phase clinical trial.
- EA pharmaceutical company is permitted to bypass the standard three-phase clinical trial if the medication in question both targets a designated rare disease and has received full regulatory approval in a recognized partner nation.
Answer
If a medication neither targets a designated rare disease nor has received full regulatory approval in a recognized partner nation, then the pharmaceutical company is not permitted to bypass the standard three-phase clinical trial.
This option accurately presents the logically valid contrapositive of the stimulus. The original statement is structured as: Bypass -> (Rare Disease OR Partner Approval). The contrapositive requires negating both sides and reversing the logical arrow. Crucially, by De Morgan's laws, negating a disjunction (Rare Disease OR Partner Approval) creates a conjunction (NOT Rare Disease AND NOT Partner Approval). Therefore, if a medication lacks both required criteria, the company is absolutely not permitted to bypass the clinical trials.
Step-by-Step Solution
Key Concept
Forming contrapositives of compound conditional statements using De Morgan's laws.
Estimated Time:1m 30s