Tap any paragraph to write a margin note. Your notes collect in the Desk below the text and file under cases with @. The side-by-side margin rail opens on a larger screen.

Code · CFR · Title 37 — Patents, Trademarks, and Copyrights · Part 1 · § 1.778

§ 1.778. Calculation of patent term extension for an animal drug product.

755 words·~3 min read·/us/cfr/t37/s§ 1.778·

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

(a)If a determination is made pursuant to § 1.750 that a patent for an animal drug is eligible for extension, the term shall be extended by the time as calculated in days in the manner indicated by this section. The patent term extension will run from the original expiration date of the patent or any earlier date set by terminal disclaimer (§ 1.321).
(b)The term of the patent for an animal drug will be extended by the length of the regulatory review period for the drug as determined by the Secretary of Health and Human Services, reduced as appropriate pursuant to paragraphs (d)(1) through (d)(6) of this section.
(c)The length of the regulatory review period for an animal drug will be determined by the Secretary of Health and Human Services. Under 35 U.S.C. 156(g)(4)(B), it is the sum of---
(1)The number of days in the period beginning on the earlier of the date a major health or environmental effects test on the drug was initiated or the date an exemption under subsection
(j)of section 512 of the Federal Food, Drug, and Cosmetic Act became effective for the approved animal drug and ending on the date an application was initially submitted for such animal drug under section 512 of the Federal Food, Drug, and Cosmetic Act; and
(2)The number of days in the period beginning on the date the application was initially submitted for the approved animal drug under subsection
(b)of section 512 of the Federal Food, Drug, and Cosmetic Act and ending on the date such application was approved under such section.
(d)The term of the patent as extended for an animal drug will be determined by---
(1)Subtracting from the number of days determined by the Secretary of Health and Human Services to be in the regulatory review period:
(i)The number of days in the periods of paragraphs (c)(1) and (c)(2) of this section that were on and before the date on which the patent issued;
(ii)The number of days in the periods of paragraphs (c)(1) and (c)(2) of this section during which it is determined under 35 U.S.C. 156(d)(2)(B) by the Secretary of Health and Human Services that applicant did not act with due diligence;
(iii)One-half the number of days remaining in the period defined by paragraph (c)(1) of this section after that period is reduced in accordance with paragraphs (d)(1)
(i)and
(ii)of this section; half days will be ignored for purposes of subtraction;
(2)By adding the number of days determined in paragraph (d)(1) of this section to the original term of the patent as shortened by any terminal disclaimer;
(3)By adding 14 years to the date of approval of the application under section 512 of the Federal Food, Drug, and Cosmetic Act;
(4)By comparing the dates for the ends of the periods obtained pursuant to paragraphs (d)(2) and (d)(3) of this section with each other and selecting the earlier date;
(5)If the original patent was issued after November 16, 1988, by---
(i)Adding 5 years to the original expiration date of the patent or any earlier date set by terminal disclaimer; and
(ii)Comparing the dates obtained pursuant to paragraphs (d)(4) and (d)(5)(i) of this section with each other and selecting the earlier date;
(6)If the original patent was issued before November 16, 1988, and
(i)If no major health or environmental effects test on the drug was initiated and no request was submitted for an exemption under subsection
(j)of section 512 of the Federal Food, Drug, and Cosmetic Act before November 16, 1988, by---
(A)Adding 5 years to the original expiration date of the patent or earlier date set by terminal disclaimer; and
(B)Comparing the dates obtained pursuant to paragraphs (d)(4) and (d)(6)(i)(A) of this section with each other and selecting the earlier date; or
(ii)If a major health or environmental effects test was initiated or a request for an exemption under subsection
(j)of section 512 of the Federal Food, Drug, and Cosmetic Act was submitted before November 16, 1988, and the application for commercial marketing or use of the animal drug was not approved before November 16, 1988, by---
(A)Adding 3 years to the original expiration date of the patent or earlier date set by terminal disclaimer, and
(B)Comparing the dates obtained pursuant to paragraphs (d)(4) and (d)(6)(ii)(A) of this section with each other and selecting the earlier date. \[54 FR 30381, July 20, 1989\]
Connectionstraces to 1
Traces to 1 document
Citation graph
cites case law
§ 1.778
Calculation of patent term extension for an animal drug product.
Cites 1Cited by 0 across 0 sources
★   the supreme law of the land   ★
Don't Tread on Me
E Pluribus Unum — out of many, one

"If you don't know your rights, you don't have any."

Marginalia · a citizen's law index
A research desk, not legal advice. Always read the cited source before relying on a summary.
Questions or an issue? support@self-law.org
disclaimerMarginalia is a research index, not a law firm. Nothing on this site is legal, tax, or financial advice and no attorney–client relationship is formed by using it. Statutes, regulations, and case law change; summaries, search results, AI output, and member posts may be incomplete, out of date, or wrong. Any interpretation drawn from material on this site should be validated by a licensed attorney in your jurisdiction before you act on it.