Louisiana 2024 2024 Regular Session

Louisiana House Bill HB815 Comm Sub / Analysis

                    DIGEST
The digest printed below was prepared by House Legislative Services.  It constitutes no part of the
legislative instrument.  The keyword, one-liner, abstract, and digest do not constitute part of the law
or proof or indicia of legislative intent.  [R.S. 1:13(B) and 24:177(E)]
HB 815 Engrossed	2024 Regular Session	Billings
Abstract:  Requires the La. Dept. of Health (LDH) to ensure that all descriptive advertising and
promotional material relating to drugs, pharmaceuticals, medical devices, or vaccinations follow
certain federal laws and rules.
Proposed law requires LDH to ensure that all descriptive advertising and promotional material
relating to drugs, pharmaceuticals, medical devices, or vaccinations follow certain federal laws and
rules.
Proposed law provides that the federal rules and regulations relative to commercial advertisement
shall apply. 
Proposed law provides that notice of noncompliance shall be given to the manufacturer of the drug,
pharmaceutical, medical device, or vaccine-related advertisement or promotional material within 30
days of such noncompliant advertisements or promotional material or within thirty days of the
determination of noncompliance. 
Proposed law requires the manufacturer to remedy its noncompliance within 30 days of receiving
notice.  
Proposed law provides that if, after notice has been received and the 30-day period has lapsed, the
drug, pharmaceutical, medical device, or vaccine-related advertisement or promotional material shall
be subject to immediate removal from display or distribution by LDH if it continues to be
noncompliant. 
Proposed law requires LDH to produce only advertisements and promotional materials that comply
with the provisions of proposed law and federal regulations. 
(Adds R.S. 40:1176.1)
Summary of Amendments Adopted by House
The Committee Amendments Proposed by House Committee on Health and Welfare to the
original bill:
1. Change references from "medical treatment" to "medical device".  2. Change references from "publication or broadcast" to "display or distribution by LDH". 
3. Remove proposed law provision that requires LDH to utilize existing staff to implement
proposed law.
4. Require all descriptive advertising and promotional material relating to drugs,
pharmaceuticals, medical devices, or vaccinations to comply with the Federal Food,
Drug, and Cosmetic Act.
5. Provide that notice of noncompliance shall be given to the manufacturer of the drug,
pharmaceutical, medical device, or vaccine-related advertisement or promotional
material within 30 days of the noncompliant advertisements or promotional material or
within 30 days of the determination of noncompliance.
6. Make technical corrections.