Adhering to ICH Q7 for GMPs

Published on: 
Pharmaceutical Technology, Pharmaceutical Technology-03-02-2013, Volume 37, Issue 3

FDA's requirements for API manufacturers in regards to ICH Q7.

Q. How closely does FDA expect API manufacturers to adhere to ICH Q7 for GMPs?




Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients

, like its ICH Q1-Q11 siblings, was developed within the designated ICH Expert Working Group and was subject to consultation by the regulatory parties, in accordance with the ICH process (1). In November 2000, ICH Q7 was endorsed by the ICH Steering Committee and subsequently adopted by the participating ICH regulatory bodies of the European Union, Japan, and the United States. It, therefore, has international adoption and acceptance. The overall ICH process is, in my opinion, the best example of successful international harmonization efforts, creating a foundation of common standards upon which meaningful leveraging opportunities may be built.

ICH Q7 itself provides guidance regarding cGMPs for the manufacturing of APIs under an appropriate system for managing quality. It is also intended to help ensure that APIs meet the quality and purity characteristics that they purport, or are represented, to possess. Legally, FDA considers ICH Q7 to be the equivalent of "guidance." FDA guidance documents are quite helpful and typically explain the agency's interpretation of laws and regulations, often describing acceptable means and methods that would comply with the law and that may be considered best practices. Although guidance documents are not legally binding, following them is highly recommended. FDA cannot enforce guidance nor will it specifically cite departures from guidance in regulatory communication. The agency enforces the law and properly promulgated regulations that have the force and effect of law. How then is ICH Q7 used by FDA in the regulation of API manufacturers?

The Federal Food, Drug and Cosmetic Act Section 501 (21 USC 351) states that a drug (whether the drug is a finished pharmaceutical or a component of a finished pharmaceutical) is considered adulterated if "...the methods used in, or the facilities or controls used for, its manufacture, processing, packing, or holding do not conform to or are not operated or administered in conformity with current good manufacturing practice..."(2). For finished pharmaceuticals, the cGMP requirements are clear—the agency promulgated cGMP regulations for finished pharmaceuticals in 21 CFR 210/211 (3).

The agency has not established cGMP regulations for APIs. Nevertheless, APIs must still meet the provisions of the law and be manufactured in conformance with cGMP. But without regulations, what is considered to be cGMP for an API? The answer, for all practical purposes, is ICH Q7 is considered to be cGMP for an API. Closely following its provisions will not only help ensure your APIs are safe, pure, and potent, but following its provisions will also help ensure your APIs are not considered to be cGMP-adulterated.


1. ICH, Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients (November 2000).

2. Federal Food, Drug and Cosmetic Act Section 501 (21 USC 351).

3. 21 CFR 210/211.