Respuesta :
A regulatory body in the health care area administers examinations and maintains a current list of qualified personnel is Registration.
All investigational new drug applications, new drug applications, product license applications, biologics license applications, or similar regulatory applications of the Company and its Subsidiaries that have been submitted to or approved by the FDA or any relevant Governmental Entity are referred to as "Regulatory Registrations."
When submitted to the FDA or other Regulatory Authority, all applications, notifications, submissions, information, claims, reports, statistics, and other data used as the basis for or submitted in connection with regulatory registrations from the FDA or other Regulatory Authority relating to the Company or their respective business operations.
This tests if the pharmaceutical products were true, accurate, and complete in all material respects as stated in or modification to such applications, submissions, information and data have been submitted to the FDA or such other Regulatory Authority.
Learn more about FDA here;
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