CFR - Code of Federal Regulations Title 21

Question 1

Compensation affected by the outcome of clinical studies

Answer 1

compensation that could be higher for a favorable outcome than for an unfavorable outcome, such as compensation that is explicitly greater for a favorable result or compensation to the investigator in the form of an equity interest in the sponsor of a covered study or in the form of compensation tied to sales of the product, such as a royalty interest.

Question 2

Significant equity interest in the sponsor of a covered study

Answer 2

means any ownership interest, stock options, or other financial interest whose value cannot be readily determined through reference to public prices (generally, interests in a nonpublicly traded corporation), or any equity interest in a publicly traded corporation that exceeds $50,000 during the time the clinical investigator is carrying out the study and for 1 year following completion of the study.

Question 3

Proprietary interest in the tested product

Answer 3

means property or other financial interest in the product including, but not limited to, a patent, trademark, copyright or licensing agreement.

Question 4

Clinical investigator

Answer 4

means only a listed or identified investigator or subinvestigator who is directly involved in the treatment or evaluation of research subjects. The term also includes the spouse and each dependent child of the investigator.

Question 5

Covered clinical study

Answer 5

means any study of a drug or device in humans submitted in a marketing application or reclassification petition subject to this part that the applicant or FDA relies on to establish that the product is effective (including studies that show equivalence to an effective product) or any study in which a single investigator makes a significant contribution to the demonstration of safety. This would, in general, not include phase l tolerance studies or pharmacokinetic studies, most clinical pharmacology studies (unless they are critical to an efficacy determination), large open safety studies conducted at multiple sites, treatment protocols, and parallel track protocols. An applicant may consult with FDA as to which clinical studies constitute “covered clinical studies” for purposes of complying with financial disclosure requirements.

Question 6

Significant payments of other sorts

Answer 6

means payments made by the sponsor of a covered study to the investigator or the institution to support activities of the investigator that have a monetary value of more than $25,000, exclusive of the costs of conducting the clinical study or other clinical studies, (e.g., a grant to fund ongoing research, compensation in the form of equipment or retainers for ongoing consultation or honoraria) during the time the clinical investigator is carrying out the study and for 1 year following the completion of the study.

Question 7

Applicant

Answer 7

means the party who submits a marketing application to FDA for approval of a drug, device, or biologic product. The applicant is responsible for submitting the appropriate certification and disclosure statements required in this part.

Question 8

Sponsor of the covered clinical study

Answer 8

means the party supporting a particular study at the time it was carried out.

Question 9

21 CFR Part 11

Answer 9

Electronic Records; Electronic Signatures

Question 10

21 CFR Part 50

Answer 10

Protection of Human Subjects

Question 11

21 CFR Part 56

Answer 11

Institutional Review Boards

Question 12

21 CFR 312

Answer 12

Investigational New Drug Application

Question 13

21 CFR 812

Answer 13

Investigational Device Exemptions