• RE: IRIS Industry Coordinator role x inspections in IRIS

    thank you for your reply. I posted this question 11 months ago. Back then, the IRIS Industry Coordinator was likely not fully functional yet. I can confirm that in the present, this role works fine for me. 
  • IRIS Industry Coordinator role x inspections in IRIS

    Hello, I'd like to ask about the IRIS Industry Coordinator role. I have tried looking for information in both this forum and the IRIS guide for applicants (How to create and submit scientific applications, for industry and individual applicants) Version 2.13 but couldn't find much. 

    Info given in EMA account management abut IRIS Industry Coordinator role:  
    "You should request this role only if you want to see and edit ALL submissions for the organization to which you are requesting affiliation, created by any other user in the organization. With this affiliation role, you are able to access those submissions, add other managers and change the portal contact (person receiving emails for the submission). This affiliation role by itself does not allow to create new submission (the Industry Manager affiliation role is necessary for that). Please note that this role is optional and should be granted by the IRIS Industry User Admin only if they are aware of the implications. The role may not be suitable for a consultant, who is acting on behalf of the organization."

    Is it possible that, having this role, I am not able to add Managers/Contributors and change the Submission Contact for a GMP inspection? Does the Portal Contact still have to do this himself/herself? 

    Thank you very much and kind regards,
    Katerina Klegova