How are you merging your data from different sources and complying with HIPAA restrictions?

I recently asked Jill Heins-Nesvold from the American Lung Association of Minnesota this question and she shared her experiences about merging data and complying with HIPAA restrictions.

How do you effectively identify partners/collaborators in order to get access to data/their data?

I asked Jill Heins-Nesvold from the American Lung Association of Minnesota for tips on how a program should identify partners and how to access their data: