RACGP Three Key Principles for the Secondary Use of General Practice Data by Third Parties

In consultation with software vendors, like Best Practice, The Royal Australian College of General Practitioners (RACGP) has recently developed resources centred around three key principles for the secondary use of general practice data by third parties. These principles are designed to ensure that patient privacy is protected and that any secondary use of the data is appropriate and ethical.

Patient privacy must be protected. This first key principle means that any use of general practice data must comply with the relevant privacy laws and regulations and that patients must give informed consent before their data can be used. In addition, any third party using the data must have appropriate security measures to prevent unauthorised access or disclosure of the data.

The second key principle is that the use of general practice data must be appropriate and ethical. Meaning that the data should only be used for purposes that are consistent with the primary purpose of the data collection, which is to support patient care. Any secondary use of the data must also be transparent, and patients must be made aware of how their data is being used. Finally, the third key principle is that general practice data should only be used for research or other secondary purposes where there is a clear public benefit. This means that any use of the data must be able to demonstrate a clear and tangible benefit to the public, such as improving patient outcomes or advancing medical research.

These principles are important because they help to ensure that patient privacy is protected and that any secondary use of general practice data is conducted appropriately and ethically. By following these principles, third parties can help build trust with patients and the wider community and ensure that the use of general practice data is seen as a positive development that benefits everyone. It is worth noting that these principles are not binding legal requirements but rather a set of guidelines that the RACGP have developed to promote best practice using general practice data. As such, they are intended to be flexible enough to accommodate different contexts and situations while providing clear guidance on handling general practice data responsibly and ethically.

In practice, this means that third parties who wish to use general practice data for research or other purposes must first obtain patients’ consent and ensure that appropriate security measures are in place to protect the data from unauthorised access or disclosure. They must also ensure that any use of the data is consistent with the primary purpose of the data collection and that there is a clear public benefit to the proposed use. These principles form an essential framework for ensuring that patient privacy is protected and that any secondary use of the data is conducted in a way that is appropriate and ethical. By following these principles, third parties can help build trust with patients and the wider community and ensure that using general practice data is a positive development that benefits everyone.

For more information and to download the RACGP’s resources, please click here.