Staying Ahead of E-prescribing Requirements
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Staying Ahead of E-prescribing Requirements
If your platform isn’t compliant with the latest industry and regulatory certifications, your customers are at risk, putting your customer retention in jeopardy as well.
Cures Act Final Rule
• By end of 2023, must meet electronic health information (EHI) export criteria
• Must use APIs to provide access to medical records
• Risk $1M fine for each violation of Information Blocking Rule1
State EPCS and PDMP Mandates
DrFirst has been at the forefront of electronic prescribing of controlled substances (EPCS) since it sent the nation’s first electronic prescription of a controlled substance. With EPCS legalized nationally, a majority of states have since mandated the use of EPCS for all controlled substances. View Map
Federal EPCS Compliance
The Centers for Medicare & Medicaid Services (CMS) delayed the mandate deadline to January 1, 2023, for the SUPPORT Act. This requires all controlled substance prescriptions under Medicare’s Part D drug plan to be transmitted electronically.
With standards and regulatory requirements changing constantly, extensive legal, compliance, and product development resources are necessary to stay current. This burden challenges your roadmap commitments, competing priorities, and already scare resources.
If your platform isn’t compliant with the latest industry and regulatory certifications, your customers are at risk, putting your customer retention in jeopardy as well.
Cures Act Final Rule
State EPCS and PDMP Mandates
DrFirst has been at the forefront of electronic prescribing of controlled substances (EPCS) since it sent the nation’s first electronic prescription of a controlled substance. With EPCS legalized nationally, a majority of states have since mandated the use of EPCS for all controlled substances. View Map
Federal EPCS Compliance
The Centers for Medicare & Medicaid Services (CMS) delayed the mandate deadline to January 1, 2023, for the SUPPORT Act. This requires all controlled substance prescriptions under Medicare’s Part D drug plan to be transmitted electronically.
With standards and regulatory requirements changing constantly, extensive legal, compliance, and product development resources are necessary to stay current. This burden challenges your roadmap commitments, competing priorities, and already scare resources.
Partners who say our software integrations improved their regulatory compliance and quality measures2
Outsource your regulatory challenges by integrating DrFirst’s solutions seamlessly with existing workflows to:
Regulatory and interoperability experts from Point-of-Care Partners discuss the complex issues surrounding policy and regulation and the impact on your organization.
Nick Barger, PharmD, knows that complying with an ever-changing regulatory environment isn’t easy. But as with everything in life, there are risks and opportunities. Here are some ways to position your company and your customers to dodge the risks while getting the biggest benefit from the opportunities.
1. Office of the National Coordinator for Health Information Technology
2. 2021 Techvalidate survey