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Med error reports to FDA show a mixed bag

GovernmentDocs 5/4/2008 | 0 (0) | 14 | 0 | 0 | English

Safety PageTable 1.Med error reports to FDA show a mixed baghe medication errors staff in... adopted by the FDA in 1999. In May 2001, the FDA received 273 reports of medication errors. Excluding  ... more>>

Med error reports to FDA show a mixed bag Medication Errors

FDADocs 5/8/2008 | 0 (0) | 22 | 0 | 0 | English

Safety PageTable 1.Med error reports to FDA show a mixed baghe medication errors staff in... adopted by the FDA in 1999. In May 2001, the FDA received 273 reports of medication errors. Excluding  ... more>>

Annual reports cover letter

FDADocs 5/9/2008 | 0 (0) | 16 | 0 | 0 | English

Meeting Report of the Food and Drug Administration (FDA) for the fiscal year 2005. A list of the Advisory Committees that held closed meetings during FY 2005 is attached. These reports are submitted  ... more>>

Annual reports cover letter

FDADocs 5/9/2008 | 0 (0) | 15 | 0 | 0 | English

Meeting Report of the Food and Drug Administration (FDA) for the fiscal year 2005. A list of the Advisory Committees that held closed meetings during FY 2005 is attached. These reports are submitted  ... more>>

Annual reports medical devices

FDADocs 5/9/2008 | 0 (0) | 21 | 0 | 0 | English

Panel provides advice to the Commissioner on complex or contested scientific issues between the FDA... applications, regulatory decisions and actions by FDA, and Agency guidance and policies. The Panel  ... more>>

Annual reports medical devices

FDADocs 5/9/2008 | 0 (0) | 22 | 0 | 0 | English

Panel provides advice to the Commissioner on complex or contested scientific issues between the FDA... applications, regulatory decisions and actions by FDA, and Agency guidance and policies. The Panel  ... more>>

Annual reports list of committees

FDADocs 5/9/2008 | 0 (0) | 14 | 0 | 0 | English

List of the Advisory Committees of the Food and Drug Administration That Held Closed Meetings Fiscal Year 2005Centerfor Biologics Evaluation and Research: Blood Products Adviso...  ... more>>

Annual reports list of committees

FDADocs 5/9/2008 | 0 (0) | 14 | 0 | 0 | English

List of the Advisory Committees of the Food and Drug Administration That Held Closed Meetings Fiscal Year 2005Centerfor Biologics Evaluation and Research: Blood Products Adviso...  ... more>>

FDA A fillable

GovernmentDocs 5/4/2008 | 0 (0) | 71 | 1 | 0 | English

reports until the FDA-assigned number is received. The distributor (importer) would still enter the... AdministrationMEDWATCHFORM FDA 3500A (10/05)A. PATIENT INFORMATION1. Patient Identifier 2. Age  ... more>>

Postmarketing Expedited Safety Reports Day Alert Reports

FDADocs 5/5/2008 | 0 (0) | 11 | 0 | 0 | English

Safety Reports – 15-Day Alert Reports Regulatory Citation: 21 CFR 310.305(c), 314.80(c... Center’s readiness to accept Postmarketing Expedited and Periodic Individual Case Safety Reports in  ... more>>

Adobe Acrobat PDF format FDA Pesticide Program ResidueMonitoring Reports

FDADocs 5/9/2008 | 0 (0) | 23 | 0 | 0 | English

pesticide reports, FDA provided Total Diet Study findings for 1987-1998 (4a, 4b). More detailed...Food and Drug Administration Pesticide Program Residue Monitoring 2002Table of ContentsFDA  ... more>>

Attachment II Summaries of Selected Adverse Reaction Reports Related to Olestra Ninth Report to the FDA

FDADocs 5/9/2008 | 0 (0) | 11 | 0 | 0 | English

- continued Summaries of Selected Adverse Reaction Reports Related to Olestra Ninth Report to the FDA.....Attachment II Summaries of Selected Adverse Reaction Reports Related to Olestra Ninth  ... more>>

Attachment II Summaries of Selected Adverse Reaction Reports Related to Olestra Ninth Report to the FDA RPT6

FDADocs 5/9/2008 | 0 (0) | 13 | 0 | 0 | English

- continued Summaries of Selected Adverse Reaction Reports Related to Olestra Ninth Report to the FDA.....Attachment II Summaries of Selected Adverse Reaction Reports Related to Olestra Ninth  ... more>>

Postmarketing Expedited Safety Reports Day Alert Reports 92S 0251

FDADocs 5/9/2008 | 0 (0) | 27 | 0 | 0 | English

Safety Reports – 15-Day Alert Reports Regulatory Citation: 21 CFR 310.305(c), 314.80(c... Center’s readiness to accept Postmarketing Expedited and Periodic Individual Case Safety Reports in  ... more>>

Attachment Number of BPD Reports by Type of Table Number of BPD Reports by Type of Blood Establishments

FDADocs 5/9/2008 | 0 (0) | 20 | 0 | 0 | English

Attachment 1 – FY06: Number of BPD Reports by Type of Blood Establishment Licensed Blood Unlicensed... BPD Reports by Type of Blood Establishment Licensed Blood Unlicensed Blood BPD CODES  ... more>>


   
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