(410 ILCS 620/21) (from Ch. 56 1/2, par. 521)
Sec. 21.
(a) The authority to promulgate regulations for the efficient
enforcement of this Act is vested in the Director. The Director is
authorized to make the regulations promulgated under this Act conform, in
so far as practicable, with those promulgated under the Federal Act.
(b) Hearings authorized or required by this Act shall be conducted by
the Director or an officer, agent or employee designated by him.
(c) All pesticide chemical regulations and supplements thereto or revisions
thereof adopted under authority
of the Federal Food, Drug and Cosmetic Act are the pesticide chemical regulations
in this State, except insofar as modified or rejected by regulations for
finished foods promulgated
by the Director.
(d) All food additive regulations and supplements thereto or revisions
thereof adopted under authority
of the Federal Food, Drug and Cosmetic Act are the
food additive regulations in this State, except insofar as modified or
rejected by regulations promulgated by the Director.
(e) All color additive regulations and supplements thereto or revisions
thereof adopted under authority
of the Federal Food, Drug and Cosmetic Act are the
color additive regulations in this State, except insofar as modified or
rejected by regulations promulgated by the Director.
(f) All special dietary use regulations and supplements thereto or revisions
thereof adopted under authority
of the Federal Food, Drug and Cosmetic
Act are the special dietary use regulations in this State, except insofar
as modified or rejected by regulations promulgated by the Director.
(g) All bottled water and vended water device regulations and
supplements thereto or revisions thereof adopted under the authority of the
Federal Food, Drug and Cosmetic Act are the bottled water and vended water
device regulations in this State except insofar as modified or rejected by
regulations promulgated by the Director.
(h) All infant formula regulations and supplements thereto or revisions
thereof adopted under the authority of the Federal Food, Drug and Cosmetic Act
are the infant formula regulations in this State except insofar as modified
or rejected by regulations promulgated by the Director.
(i) All food, drug, device and cosmetic Good Manufacturing Practices
Regulations and supplements thereto or revisions thereof adopted under the
authority of Federal Food, Drug and Cosmetic Act are the food, drug, device
and cosmetic Good Manufacturing Practices Regulations in this State, except
insofar as modified or rejected by regulations promulgated by the Director.
(j) A federal regulation automatically adopted pursuant to this Act
takes effect in this State on the date it becomes effective as a Federal
regulation. No publication or hearing is required. The Director shall promulgate
all other proposed regulations in compliance with the requirements
of The Illinois Administrative Procedure Act.
(Source: P.A. 84-891.)
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