Florence T Bourgeois
Biographic Data
| ID | 6066141 |
|---|---|
| NAME | Florence T Bourgeois |
| GIVEN NAMES | Florence T |
| FAMILY NAME | Bourgeois |
| SIGNATURE | BOURGEOIS F T |
| AFFILIATIONS | Boston Children's Hospital |
| ORCID | 0000-0001-7798-4560 |
| VERIFIED | Yes |
| TOTAL WORKS | 4 |
| TOTAL CITATIONS | 1 |
| WORKS AS AUTHOR | 4 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2013 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 1 |
The challenges of regulatory pluralism
Countries with small and/or less-resourced regulatory authorities that operate outside of a larger medical product regulatory system face a regulatory strategy dilemma. These countries may rely on foreign well-resourced regulators by recognising the regulatory decisions of large systems and following suit (regulatory reliance); alternatively, such countries may extend formal decision recognition to regulators in multiple other jurisdictions with …
Enrollment of Pediatric Patients in Covid-19 Interventional Trials
This cross-sectional study uses information gathered from ClinicalTrials.gov to assess the inclusion of children in COVID-19 interventional trials conducted in the US
Personal Protective Equipment for Covid-19
Industry influence in evidence production
In light of a number of recent drug development and marketing controversies, there is increasing public focus on the role of industry in determining how drugs are used.1–3 New methods that evaluate how funding has influenced the design, reporting, and synthesis of evidence from clinical trials have identified the breadth of industry involvement in evidence production. The downstream effects on public health remain difficult to quantify. In order …
Industry influence in evidence production
In light of a number of recent drug development and marketing controversies, there is increasing public focus on the role of industry in determining how drugs are used.1–3 New methods that evaluate how funding has influenced the design, reporting, and synthesis of evidence from clinical trials have identified the breadth of industry involvement in evidence production. The downstream effects on public health remain difficult to quantify. In order …
Personal Protective Equipment for Covid-19
Enrollment of Pediatric Patients in Covid-19 Interventional Trials
This cross-sectional study uses information gathered from ClinicalTrials.gov to assess the inclusion of children in COVID-19 interventional trials conducted in the US
The challenges of regulatory pluralism
Countries with small and/or less-resourced regulatory authorities that operate outside of a larger medical product regulatory system face a regulatory strategy dilemma. These countries may rely on foreign well-resourced regulators by recognising the regulatory decisions of large systems and following suit (regulatory reliance); alternatively, such countries may extend formal decision recognition to regulators in multiple other jurisdictions with …
Medicine (2 works) · Pharmaceutical Economics and Policy (2 works) · 2019-20 coronavirus outbreak (1 work) · Child and Adolescent Health (1 work) · Childhood Cancer Survivors' Quality of Life (1 work) · Coronavirus disease 2019 (COVID-19 (1 work) · Disease (1 work) · Environmental ethics (1 work) · Epistemology (1 work) · Health and Medical Research Impacts (1 work)