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EU clinical trial portal and database declared functional | RAPS
EU clinical trial portal and database declared functional | RAPS

Clinical Trial Regulation Update - PharSafer® - Specialists in Global  Clinical and Post Marketing Drug Safety
Clinical Trial Regulation Update - PharSafer® - Specialists in Global Clinical and Post Marketing Drug Safety

EMA: Points to consider on implications of COVID-19 on methodological  aspects of ongoing clinical trials - Meditrial Helpline
EMA: Points to consider on implications of COVID-19 on methodological aspects of ongoing clinical trials - Meditrial Helpline

EMA Webinar for SMEs and Academia on the Clinical Trials Regulation and the Clinical  Trials Information System | ERICA
EMA Webinar for SMEs and Academia on the Clinical Trials Regulation and the Clinical Trials Information System | ERICA

Patient involvement in EMA regulatory committees - EUPATI Toolbox
Patient involvement in EMA regulatory committees - EUPATI Toolbox

Assessment of the Regulatory Dialogue Between Pharmaceutical Companies and  the European Medicines Agency on the Choice of Noninferiority Margins -  Clinical Therapeutics
Assessment of the Regulatory Dialogue Between Pharmaceutical Companies and the European Medicines Agency on the Choice of Noninferiority Margins - Clinical Therapeutics

Clément Provansal on LinkedIn: Regulatory harmonisation of clinical trials  in the EU: Clinical Trials
Clément Provansal on LinkedIn: Regulatory harmonisation of clinical trials in the EU: Clinical Trials

Characteristics of Single Pivotal Trials Supporting Regulatory Approvals of  Novel Non-orphan, Non-oncology Drugs in the European Union and United  States from 2012-2016. - Abstract - Europe PMC
Characteristics of Single Pivotal Trials Supporting Regulatory Approvals of Novel Non-orphan, Non-oncology Drugs in the European Union and United States from 2012-2016. - Abstract - Europe PMC

The European Medicines Agency and the Regulation of Medicines in the  European Union - ScienceDirect
The European Medicines Agency and the Regulation of Medicines in the European Union - ScienceDirect

Clinical data publication | European Medicines Agency
Clinical data publication | European Medicines Agency

Correspondence with the European Medicines Agency | The BMJ
Correspondence with the European Medicines Agency | The BMJ

EMA's Press Briefing on Clinical Trials Regulation, 25 January 2022 /  Twitter
EMA's Press Briefing on Clinical Trials Regulation, 25 January 2022 / Twitter

Change management for the EudraVigilance system | European Medicines Agency
Change management for the EudraVigilance system | European Medicines Agency

Approval rating: how do the EMA and FDA compare? | Cancer World Archive
Approval rating: how do the EMA and FDA compare? | Cancer World Archive

Approval rating: how do the EMA and FDA compare? | Cancer World Archive
Approval rating: how do the EMA and FDA compare? | Cancer World Archive

Paediatric Clinical Trial Preparedness-EFGCP Webinar | ECRIN
Paediatric Clinical Trial Preparedness-EFGCP Webinar | ECRIN

Transparency of clinical trials and good governance should be included in  the EMA extended mandate | European Alliance for Responsible R&D and  Affordable Medicines
Transparency of clinical trials and good governance should be included in the EMA extended mandate | European Alliance for Responsible R&D and Affordable Medicines

EMA Explains Dos And Don'ts Of New Clinical Trials Portal :: Pink Sheet
EMA Explains Dos And Don'ts Of New Clinical Trials Portal :: Pink Sheet

The obligatory sharing of clinical trial data in the European Union -  datenschutz notizen | News-Blog der datenschutz nord Gruppe
The obligatory sharing of clinical trial data in the European Union - datenschutz notizen | News-Blog der datenschutz nord Gruppe

EMA calls for 'stakeholder' input on design of new clinical trials database
EMA calls for 'stakeholder' input on design of new clinical trials database

The European Medicines Agency Clinical Data Website Enables Insights I |  OAJCT
The European Medicines Agency Clinical Data Website Enables Insights I | OAJCT

Clinical trials for EMA-submitted medicines move away from US and Europe -  PMLiVE
Clinical trials for EMA-submitted medicines move away from US and Europe - PMLiVE

Positive outcome for ema's policy 0070, one year after the publication of  the clinical trial results - Portolano Cavallo
Positive outcome for ema's policy 0070, one year after the publication of the clinical trial results - Portolano Cavallo

COVID-19 vaccines: development, evaluation, approval and monitoring | European  Medicines Agency
COVID-19 vaccines: development, evaluation, approval and monitoring | European Medicines Agency

Transparency of Regulatory Data across the European Medicines Agency,  Health Canada, and US Food and Drug Administration | Journal of Law,  Medicine & Ethics | Cambridge Core
Transparency of Regulatory Data across the European Medicines Agency, Health Canada, and US Food and Drug Administration | Journal of Law, Medicine & Ethics | Cambridge Core