Common use of Regulated Uses Clause in Contracts

Regulated Uses. You acknowledge that the GxP Software has not been cleared, approved, registered or otherwise qualified (collectively, the “Approval”) by Molecular Devices with any regulatory agency for use in diagnostic or therapeutic procedures, or for any other use requiring compliance with any national, regional or state law regulating diagnostic or therapeutic products, blood products, medical devices or any similar product (hereafter collectively referred to as “Regulatory Approval”). The GxP Software may not be used for any purpose that would require any such Approval unless proper Approval is obtained. You agree that if you elect to use the GxP Software for a purpose that would subject you or the GxP Software to Regulatory Approval, you will be solely responsible for obtaining any required Approvals and otherwise ensuring that your use of the GxP Software complies with such laws, including, but not limited to your validation that the Software is working.

Appears in 2 contracts

Sources: End User License Agreement, End User License Agreement