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Generalstreik!
Drosten for Kanzler!
SOFORT!
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Würden Sie von diesem Mann eine Maske kaufen?



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HANNOVER:
Impfstoff ist in riesigen Mengen vorhanden.
Mehr als 1000 Ärzte WOLLEN impfen.
ABER MAN LÄSST SIE NICHT!

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Thalia-Chef Michael Busch will eins auf die Schnauze
TOTALBOYKOTT BEI THALIA!
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Manfred Doepp: im Fernsehen.
Seine Patienten: im Grab.
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Männer sind blöde.
Hier ist der Beweis.
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Geisteskranke Homöopathie-Anhänger sind eine ernste Gefahr für die Allgemeinheit
http://www.transgallaxys.com/~kanzlerzwo/index.php?topic=11953.0
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Das Innenministerium muß handeln:
Homöopathische 'Ärzte' als organisierte Kriminalität
Beweisstücke für die Staatsanwaltschaft
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Krieg! Krieg!

Homöopathen im Krieg!
Binnenkonsens ermordet!

Kriegsbericht von der Postfront:
Ab 6.2.2021 wird zurückstudiert!

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Was Einem die Vollidioten ohne Masken ins Gesicht pusten:



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Mindestens jeder siebente Pfaffe im Erzbistum Köln ist ein Täter



Vorsicht vor Pfaffen!
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Karma bit them in the ass:
Rogue Hoster OVH on fire
IT IS MUCH WORSE THAN EVER THOUGHT

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Author Topic: FDA: The Bioterrorism Act of 2002  (Read 4534 times)

ama

  • Jr. Member
  • *
  • Posts: 1145
FDA: The Bioterrorism Act of 2002
« on: April 18, 2008, 05:21:45 PM »

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http://www.fda.gov/oc/bioterrorism/bioact.html

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FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA

The Bioterrorism Act of 2002

Sign up for Bioterrorism Act email updates.

The Act
The events of Sept. 11, 2001,
reinforced the need to enhance
the security of the United
States. Congress responded by
passing the Public Health
Security and Bioterrorism
Preparedness and Response
Act of 2002 (the Bioterrorism
Act), which President Bush
signed into law June 12, 2002.
Complete Text: HTML; PDF
http://www.fda.gov/oc/bioterrorism/PL107-188.html

The Bioterrorism Act is
divided into five titles:

Introduction

Title I -- National Preparedness for Bioterrorism and Other
Public Health Emergencies

Title II -- Enhancing Controls on Dangerous Biological Agents and Toxins

Title III -- Protecting Safety and Security of Food and Drug Supply

Title IV -- Drinking Water Security and Safety

Title V -- Additional Provisions

FDA is responsible for carrying out certain provisions of the Bioterrorism Act, particularly Title III, Subtitle A (Protection of Food Supply) and Subtitle B (Protection of Drug Supply).

Plans for Implementing the Act

Title I (National Preparedness)
Section 123 (Animal Trials):
Federal Register Notice
View Comments
Title III (Safety of Food and Drug Supply):
Subtitle A (Food Supply Protection)
Section 301 (Security Strategy)
Section 302 (Food Adulteration)
Report to Congress: Testing for Food Adulteration (February 2005)
Section 303 (Detention)
Final Rule (June 4, 2004)
Press Release (May 27, 2004)
Fact Sheet
More Information
Section 305
(Registration)
Final Rule (PDF)
Press Release (Sept. 28, 2005)
Interim Final Rule  PDF)
Press Release (Oct 16, 2003)
Fact Sheet (Spanish version)
Questions and Answers
Test of Registration
Data Accuracy
Compliance Information
Small Entity Compliance Guide
Compliance Policy Guide
More Information
Section 306 (Records Maintenance)
Final Rule
Correction to the Final Rule (PDF)
Press Release (Dec. 6, 2004)
Qs & As Regarding Establishment and Maintenance of Records
Fact Sheet
Guidance on Records Access
More Information
Section 307 (Prior Notice)
Interim Final Rule PDF)
Fact Sheet (Spanish version)
Questions and Answers
Prior Notice System Interface
Compliance Summary Information
Small Entity Compliance Guide
Revised Compliance Policy Guide
Revised Joint FDA/Customs Plan
Prior Notice Contingency
Harmonized Tariff Schedule Codes
More Information
Section 308 (Marking)
Withdrawal of Prior Proposal
FDA Actions on Bioterrorism Legislation
Plan Summaries for Developing Bioterrorism Food
Regulations (sections 303-307)
Subtitle B (Drug Supply Protection)
Section 321 (Foreign Registration)
Section 322 (Import for Export)
Letter to Stakeholders
Federal Register Notice
Procedures Manual
Withdrawal of Prior Proposal

Title V:
Prescription Drug User Fee Act (Although not directly
related to the Bioterrorism provisions of the Act, this
program reauthorizes the fee program under which FDA
reviews and approves drugs.)

Public Participation

FDA will provide ongoing opportunities for constituents
to keep informed and involved in the agency's activities
related to developing regulations and guidances
associated with the Bioterrorism Act.
Before issuing proposed regulations on food-related
issues, the agency provided an opportunity for stakeholders to
identify concerns and suggest ways to address them. For
example, following a July 17, 2002 stakeholder letter to the
FDA foods community, the agency held a series of
meetings with consumers, industry, state and local
governments, transporters, and other key constituents to
brief them on the Bioterrorism Act's food provisions.

Register Your Food Facility

This is the Official U.S. FDA Site for Free Food Facility Registration
Important Notice
About Firms
Offering
Registration
Services
Register Online
Register via
Mail/Fax
Registration Help
Desk
Verification of
Registration
Prior Notice-Food
Imports
Information/Login
Plan for Uniform
System and
Coordinated
Timeframes
Compliance
Summary
Information
Updates on
Requirements
Help Desk
 
Recent Activities
Report to Congress:
Testing for Food
Adulteration (February
2005)
FDA Bioterrorism
Information
Counterterrorism
Bioterrorism Act
Archive
Other Bioterrorism
Act Information
White House
Customs & Border Protection

FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | Privacy | Accessibility
FDA Website Management Staff
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Logged
Kinderklinik Gelsenkirchen verstößt gegen die Leitlinien

Der Skandal in Gelsenkirchen
Hamer-Anhänger in der Kinderklinik
http://www.klinikskandal.com

http://www.reimbibel.de/GBV-Kinderklinik-Gelsenkirchen.htm
http://www.kinderklinik-gelsenkirchen-kritik.de
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