State of Illinois
92nd General Assembly
Legislation

   [ Search ]   [ PDF text ]   [ Legislation ]   
[ Home ]   [ Back ]   [ Bottom ]



92_HB2551

 
                                               LRB9204278DJpc

 1        AN ACT in relation to public health.

 2        Be  it  enacted  by  the People of the State of Illinois,
 3    represented in the General Assembly:

 4        Section 5.  The Illinois Food, Drug and Cosmetic  Act  is
 5    amended  by changing Sections 21 and 22.4 and adding Sections
 6    21.3 and 21.4 as follows:

 7        (410 ILCS 620/21) (from Ch. 56 1/2, par. 521)
 8        Sec. 21.  Enforcement of Act.
 9        (a)  The authority  to  promulgate  regulations  for  the
10    efficient  enforcement of this Act is vested in the Director.
11    The  Director  is  authorized   to   make   the   regulations
12    promulgated under this Act conform, in so far as practicable,
13    with those promulgated under the Federal Act.
14        (b)  Hearings authorized or required by this Act shall be
15    conducted  by  the  Director or an officer, agent or employee
16    designated by him.
17        (c)  All pesticide chemical regulations  and  supplements
18    thereto  or  revisions thereof adopted under authority of the
19    Federal  Food,  Drug  and  Cosmetic  Act  are  the  pesticide
20    chemical  regulations  in  this  State,  except  insofar   as
21    modified  or  rejected  by  regulations  for  finished  foods
22    promulgated by the Director.
23        (d)  All   food   additive  regulations  and  supplements
24    thereto or revisions thereof adopted under authority  of  the
25    Federal  Food,  Drug  and  Cosmetic Act are the food additive
26    regulations in this State,  except  insofar  as  modified  or
27    rejected by regulations promulgated by the Director.
28        (e)  All   color  additive  regulations  and  supplements
29    thereto or revisions thereof adopted under authority  of  the
30    Federal  Food,  Drug  and Cosmetic Act are the color additive
31    regulations in this State,  except  insofar  as  modified  or
 
                            -2-                LRB9204278DJpc
 1    rejected by regulations promulgated by the Director.
 2        (f)  All  special dietary use regulations and supplements
 3    thereto or revisions thereof adopted under authority  of  the
 4    Federal  Food,  Drug and Cosmetic Act are the special dietary
 5    use regulations in this State, except insofar as modified  or
 6    rejected by regulations promulgated by the Director.
 7        (g)  All   bottled   water   and   vended   water  device
 8    regulations and  supplements  thereto  or  revisions  thereof
 9    adopted  under  the  authority  of the Federal Food, Drug and
10    Cosmetic Act are the bottled water and  vended  water  device
11    regulations  in  this  State  except  insofar  as modified or
12    rejected by regulations promulgated by the Director.
13        (h)  All  infant  formula  regulations  and   supplements
14    thereto  or  revisions thereof adopted under the authority of
15    the Federal Food,  Drug  and  Cosmetic  Act  are  the  infant
16    formula  regulations in this State except insofar as modified
17    or rejected by regulations promulgated by the Director.
18        (i)  All   food,   drug,   device   and   cosmetic   Good
19    Manufacturing Practices Regulations and  supplements  thereto
20    or  revisions  thereof adopted under the authority of Federal
21    Food, Drug and Cosmetic Act are the food,  drug,  device  and
22    cosmetic  Good  Manufacturing  Practices  Regulations in this
23    State, except insofar as modified or rejected by  regulations
24    promulgated by the Director.
25        (j)  A  federal regulation automatically adopted pursuant
26    to this Act takes effect in this State on the date it becomes
27    effective as a Federal regulation. No publication or  hearing
28    is required. The Director shall promulgate all other proposed
29    regulations  in  compliance  with  the  requirements  of  The
30    Illinois Administrative Procedure Act.
31        (k)  On  and  after July 1, 2002, all federal regulations
32    concerning  food  and  supplements,  or  revisions   to   the
33    regulations  adopted under the authority of the Federal Food,
34    Drug and Cosmetic Act, including 21 C.F.R.  70  through  699,
 
                            -3-                LRB9204278DJpc
 1    are  the regulations concerning food in this State, except as
 2    modified or rejected by rules adopted by the Director.
 3        (l)  On and  after  July  1,  2002,  the  Department  may
 4    establish  and  assess  civil  monetary  penalties  against a
 5    license holder for violations  of  this  Act  or  regulations
 6    adopted  under  this  Act.   Before  assessing a penalty, the
 7    Department must give the alleged violator an  opportunity  to
 8    request  an  administrative  hearing  on  the  matter  of the
 9    alleged violation.   In  no  circumstances  may  any  penalty
10    exceed $1,000 per day for each day the license holder remains
11    in  violation.   All penalties collected under this Act shall
12    be deposited  into  the  Food  and  Drug  Safety  Fund.   The
13    Attorney  General  may  bring  a  civil action in the circuit
14    court to enforce the collection of a  penalty  imposed  under
15    this subsection.
16    (Source: P.A. 84-891.)

17        (410 ILCS 620/21.3 new)
18        Sec.  21.3.  Food manufacturers, processors, packers, and
19    warehouses; permits and inspections.
20        (a)  It  is  unlawful  for  any  person   to   establish,
21    maintain, conduct, or operate a food manufacturer, processor,
22    packer,   or   warehouse  within  this  State  without  first
23    obtaining a permit from the Department.
24        Permits shall  expire  on  September  30  of  each  year,
25    unless  revoked  by the Department for noncompliance with the
26    rules adopted  under  this  Act  or  discontinuation  of  the
27    facility's operation.
28        Applications  for  original  permits or renewals shall be
29    made on forms furnished by the Department and  shall  include
30    at least the following:
31             (1)  The  name  and address of the applicant, or the
32        names and addresses of the partners if  the applicant  is
33        a partnership, or the names and addresses of the officers
 
                            -4-                LRB9204278DJpc
 1        if  the  applicant  is  a  corporation,  or the names and
 2        addresses of all persons having a financial  interest  in
 3        the applicant if the applicant is a group of individuals,
 4        association, or trust; and
 5             (2)  The  name  of the food manufacturer, processor,
 6        packer  or  warehouse,  location,  mailing  address,  and
 7        telephone number.
 8        An initial, non-refundable fee of $100 must be  submitted
 9    to  the  Department with the application for a license.  Each
10    annual  renewal  application  must  be   submitted   with   a
11    non-refundable  $100  fee,  except  that each facility with a
12    license that has been expired for more than 90 days must  pay
13    a  non-refundable  $150  fee for renewal of the license.  All
14    fees collected shall be deposited  into  the  Food  and  Drug
15    Safety Fund.
16        Those   food   manufacturers,   processors,  packers,  or
17    warehouses permitted by the Department under Section 21.2  of
18    this  Act  or  under  the  Grade  A Pasteurized Milk and Milk
19    Products Act or by the  Illinois  Department  of  Agriculture
20    under the Meat and Poultry Inspection Act or the Illinois Egg
21    and  Egg Products Act are exempt from the permit fees in this
22    Section, but not from other provisions of this Act.
23        The  Department  is  authorized,  upon  request  and  the
24    non-refundable payment  of  $10  per  certificate,  to  issue
25    certificates   of  free  sale,  health  certificates,  or  an
26    equivalent, to  Illinois  food,  dairy,  drug,  cosmetic,  or
27    medical   device   manufacturers,   processors,  packers,  or
28    warehousers.  All fees collected shall be deposited into  the
29    Food and Drug Safety Fund.
30        The   Department   shall   issue  an  Illinois  shellfish
31    certificate, upon request, to shellfish firms  in  compliance
32    with the Interstate Shellfish Sanitation Conference.
33        (b)  Every Illinois food manufacturer, processor, packer,
34    or  warehouse  shall  be  inspected  by  the  Department at a
 
                            -5-                LRB9204278DJpc
 1    frequency that is necessary to ensure  compliance  with  this
 2    Act.
 3        (c)  This Section applies on and after July 1, 2002.

 4        (410 ILCS 620/21.4 new)
 5        Sec. 21.4.  Units of local government; home rule.
 6        (a)  The  regulation,  permitting, and inspection of food
 7    manufacturers, processors, packers, warehouses,  manufactured
 8    dairy   farms,   manufactured   dairy   plants,   bulk   milk
 9    hauler-samplers,    bulk   milk   pickup   tanks,   certified
10    pasteurizer sealers, and manufactured dairy products, but not
11    including food service establishments and retail food stores,
12    are exclusive powers and functions of the State.  A home rule
13    unit may not regulate these entities.    This  Section  is  a
14    denial and limitation of home rule powers and functions under
15    subsection  (h)  of  Section 6 of Article VII of the Illinois
16    Constitution.
17        (b)  This Section applies on and after July 1, 2002.

18        (410 ILCS 620/22.4) (from Ch. 56 1/2, par. 522.4)
19        Sec. 22.4. Food and Drug Safety Fund. There is created in
20    the State Treasury a special fund to be known as the Food and
21    Drug Safety Fund. All subscription, fine,  and  permit  fees,
22    certificate   fees,   and   other  moneys  collected  by  the
23    Department of Public Health under this Act shall be deposited
24    into the  Fund.  Subject  to  appropriation  by  the  General
25    Assembly,  moneys  deposited  into  this  Fund  shall be made
26    available to the Department of Public  Health  to  administer
27    the  Drug  Product  Selection Program or for other Department
28    activities related to food safety, drug safety, milk  safety,
29    or  drug  product selection. All interest that accrues on the
30    moneys in the Fund shall be deposited into the Fund.
31    (Source: P.A. 89-526, eff. 7-19-96.)

[ Top ]