Health Monitoring Process has many similarities Clinical Trials.
When is consent required more than once? For example: When a new PaaS AI supplier accesses the data? When during monitoring something new/different is monitored in the patient such as moods using a mood-tracking App? ( See https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5676196/ )
How can we design the Hyperledger Consent API to be universally used in all cases? Standardization?
API Structure is to be defined
Clinical trials use AI monitoring engine linked to a drug treatment plan?
What is the particular Treatment in Diabetes?
Which Framework is the best in Hyperledger? Fabric or Sawtooth? Criteria for the selection?