21 U.S.C. § 356k: Platform technologies

The Secretary shall establish a program for the designation of platform technologies that meet the criteria described in subsection (b). the platform technology is incorporated in, or utilized by, a drug approved under section 355 of this title or a biological product licensed under section 351 of the Public Health Service Act [ 42 U.S.C. 262 ]; preliminary evidence submitted by the sponsor of the approved or licensed drug described in paragraph (1), or a sponsor that has been granted a right of reference to data submitted in the application for such drug, demonstrates that the platform technology has the potential to be incorporated in, or utilized by, more than one drug without an adverse effect on quality, manufacturing, or safety; and data or information submitted by the applicable person under paragraph (2) indicates that incorporation or utilization of the platform technology has a reasonable likelihood to bring significant efficiencies to the drug development or manufacturing process and to the review process. A person may request the Secretary designate a platform technology as a designated platform technology concurrently with, or at any time after, submission under section 355(i) of this title or section 351(a)(3) of the Public Health Service Act [ 42 U.S.C. 262(a)(3) ] for the investigation of a drug that incorporates or utilizes the platform technology that is the subject of the request. Not later than 90 calendar days after the receipt of a request under subsection (c), the Secretary shall determine whether the platform technology that is the subject of the request meets the criteria described in subsection (b). If the Secretary determines that the platform technology meets the criteria described in subsection (b), the Secretary shall designate the platform technology as a designated platform technology and may expedite the development and review of any subsequent application submitted under section 355(b) of this title or section 351(a) of the Public Health Service Act [ 42 U.S.C. 262(a) ] for a drug that uses or incorporates the platform technology pursuant to subsection (e), as appropriate. If the Secretary determines that the platform technology does not meet the criteria under subsection (b), the Secretary shall include with the determination not to designate the technology a written description of the rationale for such determination. The Secretary may revoke a designation made under paragraph (2), if the Secretary determines that the designated platform technology no longer meets the criteria described in subsection (b). The Secretary shall communicate the determination to revoke a designation to the requesting sponsor in writing, including a description of the rationale for such determination. Nothing in this section shall prevent a product that uses or incorporates a designated platform technology from being eligible for expedited approval pathways if it is otherwise eligible under this chapter or the Public Health Service Act [ 42 U.S.C. 201 et seq.]. engaging in early interactions with the sponsor to discuss the use of the designated platform technology and what is known about such technology, including data previously submitted that is relevant to establishing, as applicable, safety or efficacy under section 355(b) of this title or safety, purity, or potency under section 351(a) of the Public Health Service Act [ 42 U.S.C. 262(a) ]; providing timely advice to, and interactive communication with, the sponsor regarding the development of the drug that proposes to use the designated platform technology to ensure that the development program designed to gather data necessary for approval or licensure is as efficient as practicable, which may include holding meetings with the sponsor and the review team throughout the development of the drug; and considering inspectional findings, including prior findings, related to the manufacture of a drug that incorporates or utilizes the designated platform technology. such data and information was submitted by the same sponsor, pursuant to the application for the drug with respect to which designation of the designated platform technology under subsection (d) was granted; or the sponsor relying on such data and information received a right of reference to such data and information from the sponsor described in paragraph (1). A sponsor of more than one application approved under section 355(b) of this title or section 351(a) of the Public Health Service Act [ 42 U.S.C. 262(a) ] for drugs that incorporate or utilize a designated platform technology may submit a single supplemental application for proposed changes to the designated platform technology that may be applicable to more than one such drug that incorporates or utilizes the same designated platform technology. Such supplemental application may cross-reference data and information submitted in other applications and may include one or more comparability protocols regarding how such changes to the platform technology would be made for each applicable drug or biological product. is incorporated in or utilized by a drug or biological product and is essential to the structure or function of such drug or biological product; can be adapted for, incorporated into, or utilized by, more than one drug or biological product sharing common structural elements; and facilitates the manufacture or development of more than one drug or biological product through a standardized production or manufacturing process or processes. The term “designated platform technology” means a platform technology that is designated as a platform technology under subsection (d). alter the authority of the Secretary to approve drugs pursuant to section 505 of this Act [ 21 U.S.C. 355 ] or license biological products pursuant to section 351 of the Public Health Service Act [ 42 U.S.C. 262 ], including standards of evidence and applicable conditions for approval or licensure under the applicable Act; or confer any new rights with respect to the permissibility of a sponsor of an application for a drug product or biological product referencing information contained in another application submitted by the holder of an approved application under section 355(c) of this title or of a license under section 351(a) of the Public Health Service Act [ 42 U.S.C. 262(a) ].