The fda is the regulatory agency in the united states that oversees the approval process for drugs, biologics, and medical devices. which need to be submitted to the fda before starting a clinical trial with an unapproved drug?

True

Explanation:

for any unapproved drug to be used for human clinical studies, the physician who developed the drug must first submit an Investigational New Drug (IND) application to the FDA.

answer; i believe the correct answer is customer,manufacturer, service provider,general public ; quality is primarily the responsibility of all all employees in the organization.

what are the statements