Lisa Wolf

7PUBLICATIONS
6CO-AUTHORS
Characterisation of biological macromoleculesAuditing and accountabilityToxicology (incl. clinical toxicology)Business process managementDisease surveillance
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Publications (7)

|Sep 07, 2026
Analysis of Suffix Use for Biosimilar Product Identification in Postmarketing Adverse Event Reporting.

|Jun 04, 2025
An Evaluation of Duplicate Adverse Event Reports Characteristics in the Food and Drug Administration Adverse Event Reporting System.

Scott Janiczak, Sarah Tanveer, Karen Tom

|Dec 02, 2022
The Food and Drug Administration's (FDA's) Drug Safety Surveillance During the COVID-19 Pandemic.

Ida-Lina Diak, Kimberley Swank, Kate McCartan

|Dec 21, 2018
Evaluation of Postmarketing Reports from Industry-Sponsored Programs in Drug Safety Surveillance.

Lisa Harinstein, Dipti Kalra, Cindy M Kortepeter

|Jan 20, 2018
Postmarketing cases of eluxadoline-associated pancreatitis in patients with or without a gallbladder.

L Harinstein, E Wu, A Brinker

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Frequent Collaborators

3 joint publications

Monica A Muñoz

2 joint publications

Scott Janiczak

1 joint publications

Ida-Lina Diak

1 joint publications

Michael D Blum