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1-7 of 7 results for FDA-1639

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Select article: Completeness of Adverse Drug Experience Reporting to the FDA: II. A Comparison of Manufacturer and Direct Reports on New Molecular Entities

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Research article

First published January, 1994

Completeness of Adverse Drug Experience Reporting to the FDA: II. A Comparison of Manufacturer and Direct Reports on New Molecular Entities

Annie L. Britt, Deanne E. Knapp

Therapeutic Innovation & Regulatory Science

Select article: Experience with the who Adverse Reaction Terminology at Searle

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Research article

First published April, 1986

Experience with the who Adverse Reaction Terminology at Searle

Irvin Strathman

Therapeutic Innovation & Regulatory Science

Select article: A Pilot Study of Electronic Submission of Periodic Reports to the FDA: Flexible Diskette Submission-Glaxo Program Development

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Research article

First published January, 1988

A Pilot Study of Electronic Submission of Periodic Reports to the FDA: Flexible Diskette Submission-Glaxo Program Development

Joel H. Dobbs

Therapeutic Innovation & Regulatory Science

Select article: Electronic Submission of Periodic Reports

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Other

First published April, 1989

Electronic Submission of Periodic Reports

Charles Anello

Therapeutic Innovation & Regulatory Science

Select article: Database Management and Reporting Systems — Foreign-Based Companies: The Glaxo Approach

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Other

First published April, 1989

Database Management and Reporting Systems — Foreign-Based Companies: The Glaxo Approach

John C. C. Talbot

Therapeutic Innovation & Regulatory Science

Select article: The Evaluation of Postmarketing Adverse Drug Experience Reports at FDA: Part I

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Research article

First published October, 1993

The Evaluation of Postmarketing Adverse Drug Experience Reports at FDA: Part I

Joyce M. Johnson, L. Ann Tanner, David Barash

Therapeutic Innovation & Regulatory Science

Select article: Completeness of Adverse Drug Experience Reporting by Manufacturers to the FDA

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Research article

First published October, 1991

Completeness of Adverse Drug Experience Reporting by Manufacturers to the FDA

Annie L. Britt, Deanne E. Knapp, Charles Anello [...]

Therapeutic Innovation & Regulatory Science

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