Conducting your study
Contractual arrangements with UHS that are required for research staff.
How an investigator site file is created for the study.
How compliance with the various governance regulations associated with the study is ensured.
What needs to be submitted during the progress of the study.
How the data should be handled.
Further information on patient medical notes guidance and label templates, 12 week exemption forms, participant information sheet templates, CV guidance and so on.