North Carolina § 106-712 Registration of biologics

North Carolina Statutes

§ 106-712 — Registration of biologics

North Carolina § 106-712

Ch. 106Agriculture

Art. 58North Carolina Biologics Law of 1981

This text of North Carolina § 106-712 (Registration of biologics) is published on Counsel Stack Legal Research, covering North Carolina primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

N.C. Gen. Stat. § 106-712 (2026).

Text

(a)No person shall offer for sale or use any biologic in North Carolina unless it is registered with the Commissioner. The registration shall be made on forms provided by the Commissioner. The forms shall require the applicant to provide information showing that the biologic:

(1)Is produced under procedures approved by the Commissioner;

(2)Is safe and noninjurious to animals when used as directed;

(3)Is labeled for proper handling, use and contents;

(4)Is produced in an establishment licensed under this Article; and

(5)Is not in violation of this Article or any rule or regulation promulgated thereunder.

(b)The application for registration shall also include a protocol of methods of production in detail which is followed in the production of the biologic, a sample of the label to be

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(a) No person shall offer for sale or use any biologic in North Carolina unless it is registered with the Commissioner. The registration shall be made on forms provided by the Commissioner. The forms shall require the applicant to provide information showing that the biologic:
(1) Is produced under procedures approved by the Commissioner;
(2) Is safe and noninjurious to animals when used as directed;
(3) Is labeled for proper handling, use and contents;
(4) Is produced in an establishment licensed under this Article; and
(5) Is not in violation of this Article or any rule or regulation promulgated thereunder.
(b) The application for registration shall also include a protocol of methods of production in detail which is followed in the production of the biologic, a sample of the label to be placed on the biologic, and any other information prescribed by the board as necessary for the implementation of this Article. (1981, c. 552, s. 1.)