Common use of Trial Data Clause in Contracts

Trial Data. Institution and Investigator will collect and submit to Sponsor or its designee all data generated in the conduct of the Trial including completed case report forms in the form and/or electronic medium supplied or specified by Sponsor or its designee (“CRFs”), X- rays, MRIs or other types of medical images, ECGs, EEGs or other types of tracings or printouts, and data summaries and other data as may be required under the Protocol (collectively, the “Trial Data”). Institution and Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. Sponsor is the exclusive owner of all Trial Data. Institution and Investigator will maintain complete and accurate medical records with respect to Trial Subjects. 6.2

Trial Data. During the course of the Trial, Institution and Investigator will collect and submit to Sponsor or its designee all data generated in the conduct of the Trial including including, without limitation, completed case report forms in the form and/or electronic medium supplied or specified by Sponsor or its designee (“CRFs”), X- X-rays, MRIs or other types of medical images, ECGs, EEGs or other types of tracings or printouts, and data summaries and other data as may be required under the Protocol (collectively, the “Trial Data”). Institution and Investigator will ensure accurate and timely collection, recording, and submission of Trial Data. Sponsor is the exclusive owner of all Trial Data. Institution and Investigator will maintain complete and accurate medical records with respect to Trial Subjects. 6.2.