GENERAL INFORMATION

How to participate

1.  Contact the research team

Contact the research team on 1800 811 326 or via sphpm-lymphoma@monash.edu

2. Apply for ethics and governance approval

We will contact you and discuss the process of obtaining ethics approval.

If required, a LaRDR team member will assist in the preparation of ethics documentation.

3. Receive site training

Once ethics approval has been obtained, the LaRDR team will provide remote or face-to-face training for site staff.

Ongoing training will be available as needed.

benefits of participating

• Allows sites to compare their results with results from all participating hospitals to identify variations in treatment and outcomes.
• Provides a centralised means of storing and accessing information about all cases of lymphoma at your site
• Provides collaborative and individual support for site data managers through data management meetings and one-on-one support.
• Provides access to de-identified, aggregated data for research and publication purposes Release of this data is dependent on the request meeting the requirements listed in the Data Access Policy and Steering Committee approval.