Analysis · Speech on a bill · beta

Frank Pallone, Jr.

Democrat on FDA Modernization Act 3.0 2026-07-20

129 words · 7 sentences · 9 clauses

Statement grade

Average 93 / 100

A score under 50 is red. Choose a measurement to see where it lost points and why; choose it again to clear.

Procedure 13%Claims 78%The ask 9%

This view breaks the statement into its steps and names what each one does.

Mr. Speaker, Procedure · 9 wordsI yield myself such time as I may consume.Procedure Mr. Speaker, Claims · 101 wordsI rise in support of H.R. 2821, the FDA Modernization Act 3.0, led by Representative Barragan and Representative Carter of Georgia.¹ The FDA Modernization Act 3.0 would require the Food and Drug Administration to update regulations to replace references to animal tests, data, studies, models, and research in specified sections of Title 21 of the Code of Federal Regulations with references to nonclinical tests.² This would bring FDA’s regulations in line with a law passed in 2022 that allowed for alternatives to animal testing in drug development, including those that leverage recent scientific advancements, such as computer modeling and cell-based assays.³ The ask · 11 wordsI encourage all my colleagues to vote ``yes’’ on H.R. 2821, Procedure · 8 wordsand I reserve the balance of my time.Procedure

At a glance

Lost points for

Switch Claims on to list the checkable claims here.

What the tags mean

Signal · 86

2 of 2 deductions are Signal

Signal checks whether every part makes a point, gives a reason, or asks for action. A low score means the speaker filled time with fluff, pleasantries, or attacks.

Throat-clearing: announcing what you are about to say, or the House’s routine business.What the tags mean “I yield myself such time as I may consume.”Procedure or throat-clearing: no claim, reason or ask.
Throat-clearing: announcing what you are about to say, or the House’s routine business.What the tags mean “and I reserve the balance of my time.”Procedure or throat-clearing: no claim, reason or ask.

Relevance · 100

0 of 2 deductions are Relevance

Relevance checks whether the speaker stays on topic and answers the question asked. A low score means the speaker dodged the issue. Measured against the bill under debate.

Nothing lost points.

Reasoning · 87

0 of 2 deductions are Reasoning

Reasoning checks for sound logic and solid support for any conclusion. A low score means the speaker made unsupported leaps or used weak arguments.

Nothing lost points.

Conclusions found · 1

Conclusion“I encourage all my colleagues to vote ``yes’’ on H.R.”

Because“The FDA Modernization Act 3.0 would require the Food and Drug Administration to update regulations to replace references to animal tests, data, studies, models,”

“and research in specified sections of Title 21 of the Code of Federal Regulations with references to nonclinical tests.”

“This would bring FDA’s regulations in line with a law passed in 2022 that allowed for alternatives to animal testing in drug development, including those that leverage recent scientific advancements, such as computer modeling and cell-based assays.”

Reason given

Respect · no score

Not checked: graded before this measurement existed. Excluded from the average.

Respect checks whether the speaker argued with people’s positions and records rather than attacking the people: insults, mockery, or bad motives assigned to them. Criticism of what someone did, however strong, is not marked.

Clarity · 100

0 of 2 deductions are Clarity

Clarity checks for plain speaking, clear ownership of actions, and honest limits on certainty. A low score means vague promises or evasive language.

Nothing lost points.

Claims · 3

This list shows the factual statements you can check for yourself: the words as said, and the claim restated to stand on its own.

1“2821, the FDA Modernization Act 3.0, led by Representative Barragan and Representative Carter of Georgia.”H.R. 2821, titled the FDA Modernization Act 3.0, is led by Representative Barragan and Representative Carter of Georgia.search
2“and research in specified sections of Title 21 of the Code of Federal Regulations with references to nonclinical tests.”The FDA Modernization Act 3.0 requires the FDA to replace references to animal tests, data, studies, models, and research in specified sections of Title 21 of the Code of Federal Regulations with references to nonclinical tests.search
3“a law passed in 2022 that allowed for alternatives to animal testing in drug development”A law passed in 2022 allowed for alternatives to animal testing in drug development.search

Analyzed on 2026-09-15