FDA's expanding postmarket authority to monitor and publicize food and consumer health product risks: the need for procedural safeguards to reduce "transparency" policy harms in the post-9/11 regulatory environment. [electronic resource]
Producer: 20091222Description: 577-98 p. digitalISSN:- 1064-590X
- Access to Information -- legislation & jurisprudence
- Animals
- Bioterrorism -- legislation & jurisprudence
- Civil Rights -- legislation & jurisprudence
- Computer Security
- Confidentiality -- legislation & jurisprudence
- Consumer Product Safety -- legislation & jurisprudence
- Dietary Supplements
- Disclosure -- legislation & jurisprudence
- Duty to Warn -- legislation & jurisprudence
- Food
- Food Contamination -- legislation & jurisprudence
- Food Industry -- legislation & jurisprudence
- Government Regulation
- Humans
- Legislation, Food
- Liability, Legal
- Mandatory Reporting
- Nonprescription Drugs
- Organizational Policy
- Privacy -- legislation & jurisprudence
- Product Recalls and Withdrawals -- legislation & jurisprudence
- Product Surveillance, Postmarketing
- Registries
- September 11 Terrorist Attacks -- legislation & jurisprudence
- Social Responsibility
- Terrorism -- legislation & jurisprudence
- United States
- United States Food and Drug Administration -- legislation & jurisprudence
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Publication Type: Journal Article
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