fda
TRANSCRIPT
![Page 1: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/1.jpg)
![Page 2: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/2.jpg)
Safety Assessment of Food Additives
Anna P. Shanklin, Ph.D.Department of Health and Human Services
U.S. Food and Drug Administration
Center for Food Safety and Applied Nutrition
Food Advisory CommitteeAdditives and Ingredients Subcommittee
LATEX ALLERGYAugust 26-28, 2003
![Page 3: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/3.jpg)
OVERVIEW
• Introduction
• Food & Drug Law
• Evaluation of Safety
• Natural Rubber Latex (NRL)
• Latex Allergy and Food Safety
• Conclusion
![Page 4: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/4.jpg)
CFSAN’s Mission• To promote and protect the public health by
ensuring that:
• The food supply is safe and wholesome and cosmetics are safe
• Food and cosmetic products are honestly and accurately labeled
![Page 5: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/5.jpg)
OFAS’s “Food Ingredients” Universe• Direct Food Ingredients
• Color Additives
• GRAS Ingredients
• Foods/Ingredients produced using modern biotechnology
• Processing Aids
• Food Irradiation Equipment
• Food Packaging/Food Contact Substances
Sweeteners; Preservatives; Fat;Nutrients; Texturizers (thickeners,Emulsifiers, etc.); Flavors
To process foodTo inspect food
In food, animal feed, drugs, cosmetics,medical devices(i.e. sutures and contact lenses)
Antimicrobials(meat and poultry Processing); Defoamers; Ion exchangeresins
Enzymes; Fiber; Proteins;Lipids; Sugars; MSG; Antimicrobials;Phytosterols/stanols; Flavors; Infant formula ingredients
Plants w/herbicide resistance or insect resistance, delayed ripening, etc.; often use GRAS concept
Coatings (paper, metal, etc); New/recycled plastics including both polymers and monomers; Paper; Adhesives; Ingredients in Pkgs.(i.e. colorants, antimicrobials, antixoxidants, etc.);Packaging material for use during food irradiation,; Food packaging “formulations”
![Page 6: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/6.jpg)
Food and Drug Law
• Federal, Food, Drug, and Cosmetic Act
FFDCA
Federal Food, Drug,
And Cosmetic Act
![Page 7: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/7.jpg)
FDA Authority
FFDCA
“The LAW”
![Page 8: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/8.jpg)
OFAS & FFDCAFood Additive Provisions
Sec. 409
Federal Food,
Drug,
And Cosmetic Act
409
![Page 9: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/9.jpg)
Regulations
LAW
NOT
Food Additive
![Page 10: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/10.jpg)
“PRE-MARKET” APPROVAL
1958 Food Additives Amendment
of FFDCA
Sec. 409
![Page 11: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/11.jpg)
What is a Food Additive?
The term ''food additive'' means any substance the
intended use of which results or may reasonably be
expected to result, directly or indirectly, in its
becoming a component or otherwise affecting the
characteristics of any food (including any substance
intended for use in producing, manufacturing, packing,
processing, preparing, treating, packaging,
transporting, or holding food;….
if such substance is not Generally Recognized As Safe,
Sec. 201(s) FFDCA: Definition
21 CFR 170.3(e)(1)
![Page 12: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/12.jpg)
What is a Food Additive?Sec. 201(s) FFDCA: Definition
• Any substance, that is reasonably expected to become a component of food as a result of its intended use,
• If such use in not Generally Recognized As Safe (GRAS)
IN SHORT
![Page 13: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/13.jpg)
Food and Drug Law• Sec. 409 Unsafe Food Additives: the use of a food additive is
unsafe, unless that use conforms to a regulation, notification, or exemption issued by FDA under Sec. 409.
• Sec. 402 Adulterated Food: a food is adulterated…if it is, or if it contains any food additive that is unsafe.
• Sec. 301 Prohibited Acts: the introduction or delivery into interstate commerce of any food that is adulterated or misbranded.
![Page 14: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/14.jpg)
MOM’S Apple Pies
Sweetner Unapproved Food Additive
Adulterated Food Interstate Commerce FDA Enforcement
Maryland Virginia
Food and Drug Law
![Page 15: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/15.jpg)
New antioxidant “Unapproved”
Antioxidant migratesAdulterated Food
[A][A]
Interstate CommerceFDA Enforcement
Dave’s Candy
Food and Drug Law
![Page 16: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/16.jpg)
Why are food additives regulated?
Unsafe Food Additive = Adulterated FoodUnapproved Food Additive = Unsafe Food AdditiveUnapproved Food Additive = Adulterated Food
![Page 17: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/17.jpg)
Food Drug & Cosmetic Act (As amended, 1958)
• Defines “food additive” w/GRAS exemption
• Requires premarket approval of new uses of food additives
• Establishes the standard of review
• Establishes the standard of safety
• Establishes formal rulemaking procedures
Sec. 409 FFDCA
![Page 18: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/18.jpg)
Food Drug & Cosmetic Act (As amended, 1958)
• Defines “food additive” w/GRAS exemption
• Requires premarket approval of new uses of food additives
• Establishes the standard of review
• Establishes the standard of safety
• Establishes formal rulemaking procedures
Sec. 409 FFDCA
![Page 19: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/19.jpg)
Food Drug & Cosmetic Act (As amended, 1958)
• Defines “food additive” w/GRAS exemption
• Requires premarket approval of new uses of food additives
• Establishes the standard of review
• Establishes the standard of safety
• Establishes formal rulemaking procedures
Sec. 409 FFDCA
![Page 20: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/20.jpg)
Standard of Review
“Fair evaluation of the data …”
![Page 21: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/21.jpg)
From the Senate Report on the“Food Additives Amendment of 1958”
“The committee has endeavored to prescribe a new statutory criterion requiring that a high standard of fairness be observed in administrative rule-making under this bill. Personal attitudes or preferences of administrative officials could not prevail on the basis of being supported by substantial evidence picked from the record without regard to other evidence of probative value in the record.”
![Page 22: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/22.jpg)
House of Representatives, Report No. 2284,“Food Additives Amendment of 1958”
• Committee on Interstate & Foreign Commerce, 85th Congress, 2nd Session, July 28, 1958
“The committee feels that the Secretary’s findings of fact and orders should not be based on isolated evidence in the record, which evidence in and of itself may be considered substantial without taking account of the contradictory evidence of equal or even greater substance…”
![Page 23: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/23.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 24: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/24.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 25: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/25.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 26: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/26.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 27: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/27.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 28: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/28.jpg)
Standard of Safety
“Reasonable certainty of no harm”
Commissioner David Kessler --- November 1995
![Page 29: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/29.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 30: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/30.jpg)
Standard of Safety
“Reasonable certainty of no Harm”
- Harm refers to Health
Man or Animal
What is Harm?
![Page 31: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/31.jpg)
Standard of Safety
“Reasonable certainty of no Harm”
What is Harm?
- Harm refers to Health
Man or Animal
![Page 32: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/32.jpg)
Standard of Safety
“Reasonable certainty of no Harm”
What is Harm?
- Harm refers to Health
Man or Animal
![Page 33: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/33.jpg)
Standard of Safety
• Petitioner burden to demonstrate a “reasonable certainty of no harm”
• FDA Assessment
![Page 34: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/34.jpg)
REASONABLE CERTAINTY OF NO HARMLegislative History of the FFDCA
The concept of safety used in this legislation involves the question of whether a substance is hazardous to the health of man or animal. Safety requires proof of a reasonable certainty that no harm will result from the proposed use of an additive.
It does not—and cannot—require proof beyond any possible doubt that no harm will result under any conceivable circumstance.
H.R. Report, No. 2284, 85th Congress (1958)
![Page 35: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/35.jpg)
REASONABLE CERTAINTY OF NO HARMLegislative History of the FFDCA
The concept of safety used in this legislation involves the question of whether a substance is hazardous to the health of man or animal. Safety requires proof of a reasonable certainty that no harm will result from the proposed use of an additive.
It does not—and cannot—require proof beyond any possible doubt that no harm will result under any conceivable circumstance.
H.R. Report, No. 2284, 85th Congress (1958)
![Page 36: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/36.jpg)
Section 409
Federal Food, Drug,
And Cosmetic Act
409
![Page 37: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/37.jpg)
Section 409 Requirements
• Any person may petition to establish safety
![Page 38: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/38.jpg)
Food Additive Petition ReviewThe Safety Decision
• It is NOT intended to ensure, nor is it possible to ensure, safety with absolute certainty:
(“Reasonable Certainty of No Harm rather than “Certainty of No Theoretical Possibility of Harm”)
• Does NOT weigh risks and benefits
• It is NOT intended to enforce or limit consumer choices.
What the evaluation is NOT:
![Page 39: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/39.jpg)
Food Additive Petition ReviewThe Safety Decision
• It DOES, in fact, ensure safety
• It IS a consensus decision made under uncertainty that provides a fair evaluation of all the data of record…
-That must protect the public health
-That will withstand scientific, procedural, and legal challenge from all sides
![Page 40: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/40.jpg)
Safety Standard
• Approvals are Safety Based Only
• Reasonable Certainty of No Harm
• Harm refers to Health of Man or Animal
• Fair Evaluation of the Entire Record
• Benefits not weighed in Safety Decision
Highlights
![Page 41: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/41.jpg)
Key Players
• Consumer Safety Officer (CSO)
• Chemistry
• Toxicology
• Environmental
CSO
C
T
E
![Page 42: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/42.jpg)
Data Requirements
• Identity
• Conditions of proposed use
• Intended technical effect
• Method for determining “quantity”
• Full reports of safety studies (data)
• Manufacturing methods
• Environmental information (NEPA)
Sec. 409 FFDCA
![Page 43: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/43.jpg)
Safety Evaluation
A “full blown” exhaustive
safety evaluation of all
appropriate studies, with agency ownership of safety decision.
![Page 44: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/44.jpg)
Safety Evaluation
• Estimation of Exposure• Proposed Conditions of Use• Concentration (safe)
• Level with no adverse effects observed toxicologically
“ The dose makes the poison”
“Key Determinant”
![Page 45: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/45.jpg)
Technical Review
• FDA scientist review data and evaluate petitioner’s safety argument
• FDA communicates with petitioner to resolve any questions and/or additional data needs
• FDA review, documentation
• FDA reaches a scientific conclusion and makes a recommendation
Key Players
![Page 46: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/46.jpg)
FDA’s Action on the Petition
• Complete the review
• Establish a Regulation
• Deny the Petition
Section 409 Requirements
![Page 47: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/47.jpg)
Other Legal Requirements
• Objections and Public Hearings
• Judicial Review
• Amendment or Repeal of Regulations
Section 409 Requirements
![Page 48: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/48.jpg)
Amendment or Repeal
INRegulation
OUTRegulation
=
![Page 49: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/49.jpg)
Legal Aspects of Food Additive Approvals
• Food Additives unsafe until FDA decision
• Regulations stipulate an identity, specifications and conditions of safe use
• Regulations do not provide specific product approvals
• Direct additives or Food-contact substance
![Page 50: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/50.jpg)
Food Additive Regulations21 CFR Parts 170-189
• General Provisions 170 & 171
• Direct Food Additive Regulations 172 & 173
• Indirect Food Additive Regulations 174-178• Irradiation of Foods 179
• Substances permitted on interim basis 180
• Prior Sanctioned Substances 181
• GRAS Ingredients 182-186
• Prohibited Substances 189
Title 21 CFR 177.2600 Rubber articles intended for repeat use
![Page 51: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/51.jpg)
Food Drug & Cosmetic Act (As amended, 1958, 1997)
• Defines “food additive” w/GRAS exemption• Requires premarket approval of new uses of food
additives• Establishes the standard of review• Establishes the standard of safety• Establishes formal rulemaking procedures
-----As amended 1997(FDAMA)-----• Defines “food contact substance”(FCS)• Establishes a premarket notification
program for FCSs
![Page 52: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/52.jpg)
Food Drug & Cosmetic Act (As amended, 1958, 1997)
• Defines “food additive” w/GRAS exemption• Requires premarket approval of new uses of food
additives• Establishes the standard of review• Establishes the standard of safety• Establishes formal rulemaking procedures
-----As amended 1997(FDAMA)-----• Defines “food contact substance”(FCS)• Establishes a premarket notification
program for FCSs
![Page 53: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/53.jpg)
Food Drug & Cosmetic Act (As amended, 1958, 1997)
• Defines “food additive” w/GRAS exemption• Requires premarket approval of new uses of food
additives• Establishes the standard of review• Establishes the standard of safety• Establishes formal rulemaking procedures
-----As amended 1997(FDAMA)-----• Defines “food contact substance”(FCS)• Establishes a premarket notification
program for FCSs
![Page 54: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/54.jpg)
What is a Food Contact Substance?
(Section 409(h)(6) of the FFDCA)
Any substance intended for use as a component of materials used in manufacturing, packing, packaging, transporting, or holding food if such use is not intended to have any technical effect in food.
![Page 55: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/55.jpg)
Food Contact Notifications
Food Additive that is subject of an effective notification
Safe food additive
![Page 56: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/56.jpg)
Brief SummaryFood Additive Approvals
• Mechanism: FFDCA---Sec. 409---Necessary Tools
• Process: Safety Evaluation---Scientific review team
• Result: Regulations, notifications, and exemptions
![Page 57: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/57.jpg)
Brief SummaryFood Additive Approvals
• Petitioner is responsible for demonstrating safety• FDA is responsible for
– Conducting a full and fair evaluation of the data and information– Issuing a regulation if FDA scientists conclude the requested use
is “SAFE”
FDAPetitioner
![Page 58: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/58.jpg)
Food Additive Regulations21 CFR Parts 170-189
• General Provisions 170 & 171
• Direct Food Additive Regulations 172 & 173
• Indirect Food Additive Regulations 174-178• Irradiation of Foods 179
• Substances permitted on interim basis 180
• Prior Sanctioned Substances 181
• GRAS Ingredients 182-186
• Prohibited Substances 189
Title 21 CFR 177.2600 Rubber articles intended for repeat use
![Page 59: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/59.jpg)
Natural Rubber Latex“NRL”
• § 172.615 Chewing gum base
• § 175.105 Adhesives
• § 175.125 Pressure-sensitive adhesives
• § 175.300 Resinous and polymeric coatings
![Page 60: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/60.jpg)
Natural Rubber Latex“NRL”
• § 177.1010 Acrylic and modified acrylic plastics, semirigid and rigid
• § 177.1200 Cellophane
• § 177.1210 Closures with sealing gaskets for food containers
• § 177.2600 Rubber articles intended for repeated use
![Page 61: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/61.jpg)
Natural Rubber Latex“NRL”
• 21 CFR 177.2600 (Feb. 1, 1963)
• Manufacture of Latex Food Service Gloves• Acceptable “indirect” food additive---FCS
• FDA Position• NRL currently “safe” food additive
![Page 62: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/62.jpg)
Natural Rubber Latex“NRL”
• Exposure ---- Response
• Allergic Reactions
• Latex Proteins
The Issues
![Page 63: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/63.jpg)
Latex Allergyand
Food Safety
Problem: Food Mediated Latex Allergic Reactions
![Page 64: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/64.jpg)
The Glove
• Barrier to Infectious Agents
• Food Contact Material
• Subject to the Law (FFDCA)
• Approval
Intended Use
Fair Evaluation
Reasonable Certainty of No Harm
Latex Allergy and Food Safety
![Page 65: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/65.jpg)
Latex Allergenic Proteins
• Indicated in Food Mediated Allergic reactions
• Constituents of an Indirect Food Additive
• FFDCA (Sec. 409)---Food & Drug Law
• Evaluation---General Safety Standard
Latex Allergy and Food Safety
![Page 66: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/66.jpg)
Standard of Safety
“Reasonable certainty of no harm”
![Page 67: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/67.jpg)
Latex Allergyand
Food Safety
Food Mediated Latex Allergic Reactions How do we address the Problem
![Page 68: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/68.jpg)
Latex Allergy and Food Safety
• Safety First
• FDA must operate under the Law (FFDCA)
• Approval --- Issuance of a Regulation
• Approvals are “safety” based only
• No explicit balancing of risks/benefits
• Amendment or Repeal --- Issuance of a Regulation
Addressing the Problem
![Page 69: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/69.jpg)
SUMMARY• Sec. 409 FFDCA---Food Additive Provisions
• Review Process
• Fair Evaluation of the Data --- “Review”
• Reasonable Certainty of No Harm --- “Safety”
• NRL---21 CFR 177.2600
![Page 70: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/70.jpg)
CONCLUSIONS
Evaluation of Safety
Food and Drug Law
Latex Allergy and Food Safety
![Page 71: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/71.jpg)
![Page 72: FDA](https://reader034.vdocuments.net/reader034/viewer/2022051108/544c7f21b1af9fa3478b47ca/html5/thumbnails/72.jpg)