Unlocking PMS API potential: Edit functionality training for MAHs, Online, European Medicines Agency, Amsterdam, the ...

The PMS team will host a workshop to provide insights and training on the Application Programming Interface (API) edit functionalities for MAHs. This session will offer an overview of API edit functionalities' capabilities, along with guidance on …

PMS PUI Training: Product data submission & bulk edit made easy, Online, European Medicines Agency, Amsterdam, the ...

The PMS team will host a webinar to provide insights and training on the new bulk edit functionality for MAHs, including a recap of key features. This session will offer an overview of PUI bulk edit functionality's capabilities, along with guidance on …

First EMA-ACRO bilateral meeting, European Medicines Agency, Amsterdam, the Netherlands, 2 September 2025

This meeting between European Medicines Agency (EMA) and ACRO is organised in the context of the EMA annual bilateral meetings with industry stakeholder organisations. The purpose of the meeting is to exchange views and promote dialogue on topics of common …

Op 18 augustus organiseert Delhaize Knokke-Heist de allereerste winkelcampagne rond Never Give Up Day.

Delhaize Knokke-Heist schrijft geschiedenis als eerste supermarkt in Europa die Never Give Up Day op tot leven brengt met een inspirerende in-store campagne. AMSTERDAM, NETHERLANDS, July 29, 2025 /⁨EINPresswire.com⁩/ -- In het hart van de …

Proba receives conditional endorsement from ICROA

Proba receives conditional endorsement from ICROA, validating its fertilizer-focused carbon programme for credible Scope 3 insetting and impact. AMSTERDAM, NETHERLANDS, July 29, 2025 /⁨EINPresswire.com⁩/ -- Proba, a carbon project certifier …

Q&A clinic on web-based electronic Application Form (eAF) functionalities for CAPs and non-CAPs variations, Online, ...

Clinical Trials Information System (CTIS) Bitesize talk: Redesign of the CTIS training material for sponsor users, ...

CTIS is the business tool of the EU Clinical Trials Regulation (Regulation (EU) No 536/2014) and it acts as a single entry point for clinical trial authorisation and supervision in the European Union (EU) and the European Economic Area (EEA).  This …

14th industry stakeholder platform on research and development support, European Medicines Agency, Amsterdam, the ...

This is the fourteenth in a series of regular meetings between regulators and representatives of industry stakeholder organisations. It addresses all areas of evidence generation along the medicine’s life-cycle and related to development support activities …

Training session on Human variations web-based electronic Application Form (eAF) for non-CAPs, Online, European ...

Starting from end of May 2025 EMA recommends the use of the PLM Portal web-based eAF for all non-CAPs human variations, where possible. This training aims to support users with the adoption of the web-based eAF and to showcase new functionalities, user …

EU Medicines Assessment - Opportunities for expert involvement, Online, European Medicines Agency, Amsterdam, the ...

This European Medicines Agency (EMA) and Heads of Medicines Agencies (HMA) webinar aims to raise awareness of the work of European Medicines Regulatory Network (EMRN) and to encourage broader expert participation in EMRN’s activities. The webinar explains …