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Andrew Bate

Showing results (71-80 of 110) with videos related to

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Drug Safety|December 13, 2023
Implementation of a Taxonomy-Based Framework for the Selection of Appropriate Drugs and Outcomes for Real-World Data Signal Detection StudiesAstrid Coste, Angel Ys Wong, Charlotte Warren-Gash, et al.
Clinical Pharmacology and Therapeutics|October 24, 2021
Use of Real-World Data and Evidence in Drug Development of Medicinal Products Centrally Authorized in Europe in 2018-2019Sini Marika Eskola, Hubertus Gerardus Maria Leufkens, Andrew Bate, et al.
Clinical Pharmacology and Therapeutics|December 21, 2025
The Rising Misuse of Pharmacovigilance Reporting Systems: A Threat to Evidence-Based MedicineCharles Khouri, Alex Hlavaty, Michele Fusaroli, et al.
Drug Safety|May 2, 2023
Identifying Safety Subgroups at Risk: Assessing the Agreement Between Statistical Alerting and Patient Subgroup RiskOlivia Mahaux, Greg Powell, François Haguinet, et al.
Clinical Pharmacology and Therapeutics|May 5, 2026
Reply to "A Comment about AI Methods that May Help Advance Pharmacovigilance"Charles Khouri, Alex Hlavaty, Michele Fusaroli, et al.
Drug Safety|March 17, 2026
9<sup>th</sup> ISoP Intelligent Automation Boston Seminar: From Innovation to Impact. Building Trustworthy AI in Pharmacovigilance 4-5 December 2025 | Cambridge, USA & VirtualOmar Aimer, Tarek A Hammad, Jan Petracek, et al.
British Journal of Clinical Pharmacology|February 5, 2026
Through the lens of marketing authorization holders: experience in use of real-world data and real-world evidence in drug development and regulatory submissions in EUSini M Eskola, Aleksandar Gigov, Hubertus G M Leufkens, et al.
Drug Safety|April 30, 2024
Timing Matters: A Machine Learning Method for the Prioritization of Drug-Drug Interactions Through Signal Detection in the FDA Adverse Event Reporting System and Their Relationship with Time of Co-exposureVera Battini, Marianna Cocco, Maria Antonietta Barbieri, et al.
Pharmacoepidemiology and Drug Safety|May 10, 2002
A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactionsEugène P van Puijenbroek, Andrew Bate, Hubert G M Leufkens, et al.
Drug Safety|March 13, 2025
Off-the-Shelf Large Language Models for Causality Assessment of Individual Case Safety Reports: A Proof-of-Concept with COVID-19 VaccinesAndrea Abate, Elisa Poncato, Maria Antonietta Barbieri, et al.
Pageof 11

Showing results (71-80 of 110) with videos related to

Sort By:
Pageof 11
Drug Safety|December 13, 2023
Implementation of a Taxonomy-Based Framework for the Selection of Appropriate Drugs and Outcomes for Real-World Data Signal Detection StudiesAstrid Coste, Angel Ys Wong, Charlotte Warren-Gash, et al.
Clinical Pharmacology and Therapeutics|October 24, 2021
Use of Real-World Data and Evidence in Drug Development of Medicinal Products Centrally Authorized in Europe in 2018-2019Sini Marika Eskola, Hubertus Gerardus Maria Leufkens, Andrew Bate, et al.
Clinical Pharmacology and Therapeutics|December 21, 2025
The Rising Misuse of Pharmacovigilance Reporting Systems: A Threat to Evidence-Based MedicineCharles Khouri, Alex Hlavaty, Michele Fusaroli, et al.
Drug Safety|May 2, 2023
Identifying Safety Subgroups at Risk: Assessing the Agreement Between Statistical Alerting and Patient Subgroup RiskOlivia Mahaux, Greg Powell, François Haguinet, et al.
Clinical Pharmacology and Therapeutics|May 5, 2026
Reply to "A Comment about AI Methods that May Help Advance Pharmacovigilance"Charles Khouri, Alex Hlavaty, Michele Fusaroli, et al.
Drug Safety|March 17, 2026
9<sup>th</sup> ISoP Intelligent Automation Boston Seminar: From Innovation to Impact. Building Trustworthy AI in Pharmacovigilance 4-5 December 2025 | Cambridge, USA & VirtualOmar Aimer, Tarek A Hammad, Jan Petracek, et al.
British Journal of Clinical Pharmacology|February 5, 2026
Through the lens of marketing authorization holders: experience in use of real-world data and real-world evidence in drug development and regulatory submissions in EUSini M Eskola, Aleksandar Gigov, Hubertus G M Leufkens, et al.
Drug Safety|April 30, 2024
Timing Matters: A Machine Learning Method for the Prioritization of Drug-Drug Interactions Through Signal Detection in the FDA Adverse Event Reporting System and Their Relationship with Time of Co-exposureVera Battini, Marianna Cocco, Maria Antonietta Barbieri, et al.
Pharmacoepidemiology and Drug Safety|May 10, 2002
A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactionsEugène P van Puijenbroek, Andrew Bate, Hubert G M Leufkens, et al.
Drug Safety|March 13, 2025
Off-the-Shelf Large Language Models for Causality Assessment of Individual Case Safety Reports: A Proof-of-Concept with COVID-19 VaccinesAndrea Abate, Elisa Poncato, Maria Antonietta Barbieri, et al.
Pageof 11