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| | 10100HB0342ham001 | - 2 - | LRB101 04865 RPS 56199 a |
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1 | | using a human fetal or
embryonic cell line, protein, |
2 | | deoxyribonucleic acid, recombinant
deoxyribonucleic acid, |
3 | | monoclonal antibody, or any other component
derived from an |
4 | | elective abortion or using a cell line derived from
the |
5 | | tissue of a fetus that was electively aborted. |
6 | | (b) The Department shall create and maintain a
list of each |
7 | | immunizing agent derived from aborted fetal tissue. If
an |
8 | | immunizing agent that is not an immunizing agent derived from
|
9 | | aborted fetal tissue is available as an alternative to an
|
10 | | immunizing agent derived from aborted fetal tissue, the |
11 | | Department
shall include the alternative on the list. The |
12 | | Department shall
update the list annually and make the list |
13 | | available to the public
on the Department's website. |
14 | | (c) The Department shall ensure that, beginning January 1, |
15 | | 2020, before administering an immunizing agent derived from |
16 | | aborted fetal tissue to an individual, a health care provider |
17 | | shall notify the individual or, if the individual is a child, |
18 | | the parent or guardian of the child that the immunizing agent |
19 | | was derived from aborted fetal tissue. If an immunizing agent |
20 | | that is not an immunizing agent derived from aborted fetal |
21 | | tissue is available as an alternative to an immunizing agent |
22 | | derived from aborted fetal tissue, the health care provider |
23 | | shall offer the alternative to the individual or, if the |
24 | | individual is a child, to the parent or guardian of the child. |
25 | | A health care provider shall also notify the individual or, if |
26 | | the individual is a child, the parent or guardian of the child |