# 21 CFR § 315.5: Evaluation of effectiveness

> Federal · Regulations · In force

URL: https://www.frixlaw.com/law-library/statutes/ecfr-21-315.5

## Section

- **Citation:** 21 CFR § 315.5
- **Heading:** Evaluation of effectiveness
- **Jurisdiction:** Federal
- **Kind:** Regulations
- **Status:** In force
- **Text as of:** September 22, 2026
- **Source:** Publisher's official text
- **Location:** Title 21—Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER D—DRUGS FOR HUMAN USE > PART 315—DIAGNOSTIC RADIOPHARMACEUTICALS

## Text

(a) The effectiveness of a diagnostic radiopharmaceutical is assessed by evaluating its ability to provide useful clinical information related to its proposed indications for use. The method of this evaluation varies depending upon the proposed indication(s) and may use one or more of the following criteria:
(1) The claim of structure delineation is established by demonstrating in a defined clinical setting the ability to locate anatomical structures and to characterize their anatomy.
(2) The claim of functional, physiological, or biochemical assessment is established by demonstrating in a defined clinical setting reliable measurement of function(s) or physiological, biochemical, or molecular process(es).
(3) The claim of disease or pathology detection or assessment is established by demonstrating in a defined clinical setting that the diagnostic radiopharmaceutical has sufficient accuracy in identifying or characterizing the disease or pathology.
(4) The claim of diagnostic or therapeutic patient management is established by demonstrating in a defined clinical setting that the test is useful in diagnostic or therapeutic patient management.
(5) For a claim that does not fall within the indication categories identified in § 315.4, the applicant or sponsor should consult FDA on how to establish the effectiveness of the diagnostic radiopharmaceutical for the claim.
(b) The accuracy and usefulness of the diagnostic information is determined by comparison with a reliable assessment of actual clinical status. A reliable assessment of actual clinical status may be provided by a diagnostic standard or standards of demonstrated accuracy. In the absence of such diagnostic standard(s), the actual clinical status must be established in another manner, e.g., patient followup.

## Nearby sections

- [21 CFR § 315.1 § 315.1 Scope.](https://www.frixlaw.com/law-library/statutes/ecfr-21-315.1.md)
- [21 CFR § 315.2 § 315.2 Definition.](https://www.frixlaw.com/law-library/statutes/ecfr-21-315.2.md)
- [21 CFR § 315.3 § 315.3 General factors relevant to safety and effectiveness.](https://www.frixlaw.com/law-library/statutes/ecfr-21-315.3.md)
- [21 CFR § 315.4 § 315.4 Indications.](https://www.frixlaw.com/law-library/statutes/ecfr-21-315.4.md)
- [21 CFR § 315.5 § 315.5 Evaluation of effectiveness.](https://www.frixlaw.com/law-library/statutes/ecfr-21-315.5.md)
- [21 CFR § 315.6 § 315.6 Evaluation of safety.](https://www.frixlaw.com/law-library/statutes/ecfr-21-315.6.md)
- [21 CFR § 317.2 § 317.2 List of qualifying pathogens that have the potential to pose a serious threat to public health.](https://www.frixlaw.com/law-library/statutes/ecfr-21-317.2.md)
- [21 CFR § 329.100 § 329.100 Postmarketing reporting of adverse drug events under section 760 of the Federal Food, Drug, and Cosmetic Act.](https://www.frixlaw.com/law-library/statutes/ecfr-21-329.100.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/ecfr-21-315.5. Check the current official text before relying on it. Not legal advice.