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Forum Info:

EMA will regularly publish updates on new features of IRIS. On the top of the threads list you will find "sticky" threads, containing guidelines and standard information. Please do not post confidential information in the forum.
Thread Author Last post Replies
Sticky Q&As on IRIS registration, login and RPI requests Paolo Tomasi
Paolo Tomasi
4
test Chanda Singh
Chanda Singh
0
New requirements for RPIs (domain, nature of the active substance) Paolo Tomasi
Paolo Tomasi
2
Answers to questions from Industry at the H-EG Stakeholder Meeting (Nov 2020) Paolo Tomasi
Paolo Tomasi
0
IRIS Release Information - Week of 18 January 2021 (R2.5) Paolo Tomasi
Paolo Tomasi
0
IRIS Release Information - Week of 7 December (R2.3) Carlotte Lucas
Paolo Tomasi
2
Name review request in IRIS? Ji Young Kim
Paolo Tomasi
1
Orphan annual report submission Hayley West
Paolo Tomasi
1
IRIS release information - Week of 23 November (R2.2) Paolo Tomasi
Paolo Tomasi
0
Clarifications on the "IRIS Individual user" role Paolo Tomasi
Paolo Tomasi
0
IRIS Release Information - Week of 9 November Carlotte Lucas
Carlotte Lucas
0
IRIS Release Information - Week of 14 September 2020 Carlotte Lucas
Paolo Tomasi
2
Online training on submitting scientific advice applications (human medicines) published Paolo Tomasi
Paolo Tomasi
0
Scientific Advice go-live update including training schedule Carlotte Lucas
Paolo Tomasi
3
New "IRIS General Manager" role (to view all applications from an organization) Isha Arora
Paolo Tomasi
3
Clarifications on the "IRIS Industry User Admin" role Paolo Tomasi
Paolo Tomasi
0
IRIS Industry portal has a new look and is now accepting Scientific Advice submissions Paolo Tomasi
Paolo Tomasi
0
Q&A on Scientific Advice submissions in IRIS Paolo Tomasi
Paolo Tomasi
4
Preview of the new IRIS Guideline for Applicants Paolo Tomasi
Paolo Tomasi
0
IRIS Release Information - Week of 28 September 2020 Carlotte Lucas
Carlotte Lucas
0

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