Regulatory bodies
|
Authorize or require specific PGx tests. |
Provide guidelines and/or drug labeling. |
Monitor implementation. |
Communicate with hospital leadership and payers. |
Hospital leadership
|
Secure funds and infrastructure. |
Lead the process and identify early adopters of change. |
Ensure compliance with ethical, legal and social issues. |
Monitor and evaluate the program’s impact. |
Contribute to and lead new policies. |
Communicate with regulatory bodies, payers, and pharmacy and therapeutics committee. |
Pharmacy & Therapeutics Committee
|
Evaluate the available evidence in consultation with PGx consortia and networks. |
Review the most relevant drugs. |
Narrow down to the most actionable drug-gene pairs with related variant alleles. |
Monitor and evaluate the program for improvement. |
Communicate with hospital leadership, laboratory, information technology and healthcare providers. |
Laboratory
|
Perform genotyping. |
Apply reactive point of care or preemptive testing. |
Choose candidate vs. panel testing. |
Communicate with pharmacy and therapeutics committee, information technology and healthcare providers. |
Information Technology
|
Report and integrate results into electronic health records. |
Design clinical decision support systems. |
Communicate with pharmacy and therapeutics committee, laboratory, and healthcare providers. |
Healthcare provider
|
Order the test. |
Understand and interpret the test results. |
Make therapeutic decisions. |
Educate the community. |
Communicate with patients, pharmacy and therapeutics committee, laboratory, and information technology. |
Patient
|
Provide feedback on drug outcome |
Communicate with payers and healthcare providers. |
Payer
|
Reimburse (or not) the test partially or fully |
Communicate with regulatory bodies, hospital leadership and patients. |