Change control requirements for new HPLC installation

What are the change control requirements for installation and qualification of a New HPLC instrument in QC laboratory…?

Pre-approval: URS , PO copy, Action Plan.
Post approval: IQ, OQ, PQ Qualification documents, CSV documents, Training, system equivalency (Performance) other affected Master list, calibration list, PM list, layout etc…

Is anything required other than above, pre and post approval of change control…?