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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&A on Scientific Advice submissions in IRIS
4
Sticky Q&As on IRIS registration, login and RPI requests
4
IRIS Release Information - Week of 7 December (R2.3)
0
Orphan annual report submission
1
IRIS release information - Week of 23 November (R2.2)
0
Clarifications on the "IRIS Individual user" role
0
IRIS Release Information - Week of 9 November
0
IRIS Release Information - Week of 14 September 2020
2
Online training on submitting scientific advice applications (human medicines) published
0
Scientific Advice go-live update including training schedule
3
New "IRIS General Manager" role (to view all applications from an organization)
3
Clarifications on the "IRIS Industry User Admin" role
0
IRIS Industry portal has a new look and is now accepting Scientific Advice submissions
0
Preview of the new IRIS Guideline for Applicants
0
IRIS Release Information - Week of 28 September 2020
0
Recording and presentation of access to IRIS and Research Product Identifiers (RPI) training
0
New requirements for RPIs (domain, nature of the active substance)
0
Deadlines for resubmission implemented in IRIS
0

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