If you are looking for ema adr portal, simply check out our links below :
1. European database of suspected adverse drug reaction reports
http://www.adrreports.eu/en/
The European Medicines Agency publishes these data so that its stakeholders, including the general public, can access information that European regulatory…
2. European database of suspected adverse drug reaction reports
http://www.adrreports.eu/
As of 1.2.2020, the UK is no longer an EU Member State. However, EU law still applies to the UK during the transition period. EMA. EudraVigilance.
3. ADRreports.eu portal – European Medicines Agency – europa.eu
http://www.ema.europa.eu/docs/en_GB/document_library/Presentation/2017/01/WC500219436.pdf
Understand the utility of the ADRreports.eu portal and what … The European Medicines Agency (EMA) plays a key role in the safety monitoring of medicines in…
4. User guide for online access to ADR website
https://www.ema.europa.eu/documents/regulatory-procedural-guideline/eudravigilance-european-database-suspected-adverse-reactions-related-medicines-user-manual-online_en.pdf
22 Nov 2017 – The EMA publishes the data available on the adrreports.eu portal so that its stakeholders, including the general public, can access information…
5. EudraVigilance auditable requirements project: ADRreports …
https://www.ema.europa.eu/en/ema-redirect?redirect_type=document&lang=en&doc_id=WC500222341&doc_ext=pdf
Introduction to the ADRreports.eu portal … ➢The European Medicines Agency (EMA) plays a key role in the safety monitoring of medicines in the European…
6. EudraVigilance | European Medicines Agency
https://www.ema.europa.eu/en/human-regulatory/research-development/pharmacovigilance/eudravigilance
The European Medicines Agency (EMA) operates the system on behalf of the European Union (EU) medicines regulatory network. EudraVigilance supports safe…
7. European database of suspected adverse drug reaction reports
https://data.europa.eu/euodp/en/data/dataset/suspected-adverse-drug-reaction-reports
10 Jan 2019 – EUROPAEU Open Data Portal Data Publisher European Medicines Agency European database of suspected a… Home · Data · Applications…
8. EudraVigilance: electronic reporting | European Medicines …
https://www.ema.europa.eu/en/human-regulatory/research-development/pharmacovigilance/eudravigilance/eudravigilance-electronic-reporting
In addition, EMA supports initial testing of software/system solutions by IT … reporting of ADRs directly into the EudraVigilance database means that EMA no…
9. Access to EudraVigilance data | European Medicines Agency
https://www.ema.europa.eu/en/human-regulatory/research-development/pharmacovigilance/eudravigilance/access-eudravigilance-data
EMA implemented a further minor technical update of Annex B of the policy in September 2016. The revised policy entered into force following the launch of the…
10. EudraVigilance Go-Live Plan – European Medicines Agency
https://www.ema.europa.eu/en/ema-redirect?redirect_type=jsp&webContentId=WC500235774
13 Oct 2017 – The European Medicines Agency (EMA) will launch a new and … The adrreports.eu portal website will remain live, based on the latest monthly…
11. Mandatory e-reporting essentials – EudraVigilance …
https://eudravigilance.ema.europa.eu/human/index.asp
… evaluating suspected adverse drug reactions (ADRs) during the development, … European Medicines Agency (EMA), National Competent Authorities (NCAs),…
12. EudraVigilance training and support | European Medicines …
https://www.ema.europa.eu/en/human-regulatory/research-development/pharmacovigilance/eudravigilance/eudravigilance-training-support
The European Medicines Agency (EMA) offers training to support stakeholders in … for online access via the adrreports.eu portal – Version 2.0 (PDF/1017.67 KB).