Deborah Myers
- Role
- Safety Evaluator, Division of Medication Error Prevention & Analysis, Cder at FDA
- Location
- Silver Spring, MD, US
- LinkedIn followers
- 500 followers
Experience
Safety Evaluator, Division of Medication Error Prevention & Analysis, Cder
Dec 2014 — Present · DC, US
Division of Medication Error Prevention and Analysis (DMEPA) reviews medication error reports on marketed human drugs including prescription drugs, generic drugs, and over-the-counter drugs.The DMEPA includes a medication error prevention program staffed with healthcare professionals. Among their many duties, program staff review medication error reports sent to MedWatch, evaluate causality, and analyze the data to provide solutions to reduce the risk of medication errors to industry and others at FDA. DMEPA prospectively reviews proprietary names, labeling, packaging, and product design prior to drug approval to help prevent medication errors.
Education
Ohio Northern University
BS Pharm, BS Biology, Pharmacy and Biology
The Ohio State University Fisher College of Business
MBA
2003 — 2005
Skills
- Pharmacy
- Healthcare Management
- Healthcare Information Technology
- Pharmacists
- Gcp
- Patient Safety
- Managed Care
- Hospitals
- Healthcare
- Medicine
- Healthcare Information Technology (Hit)
- Clinical Research
- Software Documentation
- Process Improvement
- Management
- Pharmaceutical Industry
- Business Process Improvement
- Clinical
- Strategy
- Regulatory Affairs
- Strategic Planning
- Quality Assurance
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