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HHS - 21 CFR PART 4

REGULATION OF COMBINATION PRODUCTS

active, Most Current
Organization: HHS
Publication Date: 1 April 2019
Status: active
Page Count: 7
scope:

What is the scope of this subpart?

This subpart applies to combination products. It establishes which current good manufacturing practice requirements apply to these products. This subpart clarifies the application of current good manufacturing practice regulations to combination products, and provides a regulatory framework for designing and implementing the current good manufacturing practice operating system at facilities that manufacture co-packaged or single-entity combination products.

Document History

April 1, 2020
REGULATION OF COMBINATION PRODUCTS
What is the scope of this subpart? This subpart applies to combination products. It establishes which current good manufacturing practice requirements apply to these products. This subpart clarifies...
21 CFR PART 4
April 1, 2019
REGULATION OF COMBINATION PRODUCTS
What is the scope of this subpart? This subpart applies to combination products. It establishes which current good manufacturing practice requirements apply to these products. This subpart clarifies...
April 1, 2018
REGULATION OF COMBINATION PRODUCTS
What is the scope of this subpart? This subpart applies to combination products. It establishes which current good manufacturing practice requirements apply to these products. This subpart clarifies...
April 1, 2017
REGULATION OF COMBINATION PRODUCTS
A description is not available for this item.
April 1, 2016
REGULATION OF COMBINATION PRODUCTS
A description is not available for this item.
April 1, 2015
REGULATION OF COMBINATION PRODUCTS
What is the scope of this subpart? This subpart applies to combination products. It establishes which current good manufacturing practice requirements apply to these products. This subpart clarifies...
April 1, 2014
REGULATION OF COMBINATION PRODUCTS
A description is not available for this item.

References

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