We have upgraded the IIS Portal to a new platform to provide you with a better user experience. The new IIS Portal is open as of 09h00 CET on April 30. Please submit new submissions using this link.
This portal is now closed for non-US applications to migrate all records to the new platform. Should you have any ongoing submissions and would like to make any changes or have questions, please contact your Roche representative or contact us at email@example.com.
Welcome to the Roche Investigator Initiated Studies Portal
Investigator Initiated Studies (IIS) are clinical studies initiated and managed by a non-pharmaceutical company researcher (e.g. individual investigator, institution, collaborative study group, cooperative group) who takes on the ethical, legal and regulatory responsibilities of the trial sponsor for the conduct and management of the study as defined by all applicable laws and regulations. By submitting your IIS proposal through this site, you are seeking support from Roche for your IIS.
The Roche IIS program is not an unrestricted grant program. There are contractual obligations tied to the receipt of any support for an IIS. IIS concept submissions will be reviewed collectively by a Roche Review Committee. Roche will inform the requester about the outcome and should Roche be interested in the concept submission, the investigator will be contacted by Roche and invited to submit further details and a full protocol on the IIS, which will be further evaluated before a final decision for support is made. Please note that submission of an IIS proposal does not guarantee support from Roche.
Please click here
to download the IIS Sponsor Reference Guide for information on how to register and submit studies.
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