<--- Back to Details
First PageDocument Content
Food and Drug Administration / Clinical research / Pharmaceuticals policy / Pharmaceutical industry / Abbreviated New Drug Application / New Drug Application / Federal Food /  Drug /  and Cosmetic Act / Ondansetron / Bioequivalence / Pharmaceutical sciences / Pharmacology / Medicine
Date: 2004-12-27 14:08:29
Food and Drug Administration
Clinical research
Pharmaceuticals policy
Pharmaceutical industry
Abbreviated New Drug Application
New Drug Application
Federal Food
Drug
and Cosmetic Act
Ondansetron
Bioequivalence
Pharmaceutical sciences
Pharmacology
Medicine

OL~~ON, PHILIP C. OLSSON RICHARD L. FRANK DAVID E WEEDA[removed]DENNIS R JOHNSON ARTHUR ‘r: TSIEN

Add to Reading List

Source URL: www.fda.gov

Download Document from Source Website

File Size: 541,98 KB

Share Document on Facebook

Similar Documents

NEWS  The Cosmetics Industry OVERVIEW In the United States cosmetics are officially regulated by the Food & Drug Administration as a result of the Food, Drug and Cosmetic Act passed inThere is also a self-regulato

NEWS The Cosmetics Industry OVERVIEW In the United States cosmetics are officially regulated by the Food & Drug Administration as a result of the Food, Drug and Cosmetic Act passed inThere is also a self-regulato

DocID: 1uASt - View Document

Evaluation of Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act Guidance for Industry

Evaluation of Bulk Drug Substances Nominated for Use in Compounding Under Section 503B of the Federal Food, Drug, and Cosmetic Act Guidance for Industry

DocID: 1tBOU - View Document

RETAIL COMPLIANCE CHECK INSPECTIONS AND FDA ACTIONS: AN OVERVIEW FOR TOBACCO RETAILERS Presented by Michelle Jackson

RETAIL COMPLIANCE CHECK INSPECTIONS AND FDA ACTIONS: AN OVERVIEW FOR TOBACCO RETAILERS Presented by Michelle Jackson

DocID: 1roDS - View Document

Use of Standards in FDA Regulatory Oversight of Next Generation Sequencing (NGS)-Based In Vitro Diagnostics (IVDs) Used for Diagnosing Germline Diseases - Draft Guidance for Stakeholders and Food and Drug Administration

Use of Standards in FDA Regulatory Oversight of Next Generation Sequencing (NGS)-Based In Vitro Diagnostics (IVDs) Used for Diagnosing Germline Diseases - Draft Guidance for Stakeholders and Food and Drug Administration

DocID: 1rmMY - View Document

Design Considerations and Pre-market Submission Recommendations for Interoperable Medical Devices - Draft Guidance for Industry and Food and Drug Administration Staff

Design Considerations and Pre-market Submission Recommendations for Interoperable Medical Devices - Draft Guidance for Industry and Food and Drug Administration Staff

DocID: 1r7Xt - View Document