Agnes Raymond-Saint

30 Churchill Place, Canary Wharf
London, ENG E145EU, United Kingdom

Last Updated: 09/26/2026

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Found 27 publications

Global Cancer Drug Development-A Report From the 2022 Accelerating Anticancer Agent Development and Validation Meeting.

Global Cancer Drug Development-A Report From the 2022 Accelerating Anticancer Agent Development and Validation Meeting.

Journal: JCO global oncology

Published: November 09, 2023

Reliance is key to effective access and oversight of medical products in case of public health emergencies.

Reliance is key to effective access and oversight of medical products in case of public health emergencies.

Journal: Expert review of clinical pharmacology

Published: August 10, 2022

WHO collaborative registration procedure using stringent regulatory authorities' medicine evaluation: reliance in action?

WHO collaborative registration procedure using stringent regulatory authorities' medicine evaluation: reliance in action?

Journal: Expert review of clinical pharmacology

Published: February 08, 2022

Assuring Access to Safe Medicines in Pregnancy and Breastfeeding.

Assuring Access to Safe Medicines in Pregnancy and Breastfeeding.

Journal: Clinical pharmacology and therapeutics

Published: January 07, 2021

Reliance: a smarter way of regulating medical products - The IPRP survey.

Reliance: a smarter way of regulating medical products - The IPRP survey.

Journal: Expert review of clinical pharmacology

Published: December 23, 2020

Remdesivir emergency approvals: a comparison of the U.S., Japanese, and EU systems.

Remdesivir emergency approvals: a comparison of the U.S., Japanese, and EU systems.

Journal: Expert review of clinical pharmacology

Published: September 10, 2020

The European Medicines Agency facilitates access to medicines in low- and middle-income countries.

The European Medicines Agency facilitates access to medicines in low- and middle-income countries.

Journal: Expert review of clinical pharmacology

Published: February 14, 2020

Are the European Medicines Agency, US Food and Drug Administration, and Other International Regulators Talking to Each Other?

Are the European Medicines Agency, US Food and Drug Administration, and Other International Regulators Talking to Each Other?

Journal: Clinical pharmacology and therapeutics

Published: June 10, 2019

Paediatric extrapolation: A necessary paradigm shift.

Paediatric extrapolation: A necessary paradigm shift.

Journal: British journal of clinical pharmacology

Published: September 18, 2018

What to Know About Medicines With New Active Ingredients Approved in FY 2016 / 2016 in Japan and EU: A Brief Comparison of New Medicines Approved in Japan and the EU in 2016.

What to Know About Medicines With New Active Ingredients Approved in FY 2016 / 2016 in Japan and EU: A Brief Comparison of New Medicines Approved in Japan and the EU in 2016.

Journal: Therapeutic innovation & regulatory science

Published: May 02, 2018

Adaptive designs in clinical trials: from scientific advice to marketing authorisation to the European Medicine Agency.

Adaptive designs in clinical trials: from scientific advice to marketing authorisation to the European Medicine Agency.

Journal: Trials

Published: March 23, 2018

Availability of paediatric information in European Medicines Agency approvals.

Availability of paediatric information in European Medicines Agency approvals.

Journal: The Lancet. Child & adolescent health

Published: February 27, 2018

Showing 1-12 of 27

Last Updated: 09/26/2026