CLINICAL TRIAL AGREEMENT This CLINICAL TRIAL AGREEMENT (the“Agreement”) is effective on the date of last signature and effective on the date of by publishing in accordance with the Act no. 340/2015 Coll. On the Register of Contracts (the “Effective...Clinical Trial Agreement • February 6th, 2020
Contract Type FiledFebruary 6th, 2020this Agreement may be terminated by PRA as provided herein. (b) The Institution shall provide appropriate resources and facilities so the Investigator can conduct the Study in a timely and professional manner and according to the terms of this Agreement. The Site shall ensure that only individuals who are appropriately trained and qualified will assist in conducting the Study. The Site is responsible for ensuring that all personnel participating in the Study (“Study Team”) comply with the terms of this Agreement. Institution and Investigator agree to promptly notify PRA in the event any Study Team Member is reported to or comes under investigation by any licensing board, independent ethics committee or institutional review board, and further agrees to promptly discontinue the use of any such personnel in connection with the Study unless PRA consents in writing to the continued use of such personnel, which such consent shall not be unreasonable delayed, conditioned, or withheld. Unless