Difference between revisions of "E9-31216 TOC"
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[[E9-31216 I D]] | [[E9-31216 I D]] | ||
== II. Overview of the Interim Final Rule == | == II. Overview of the Interim Final Rule == | ||
| − | + | [[E9-31216 II]] | |
== III. Section-By-Section Description of the Interim Final Rule == | == III. Section-By-Section Description of the Interim Final Rule == | ||
Revision as of 22:02, 27 January 2010
Contents
- 1 Table of Contents
- 1.1 I. Background
- 1.1.1 A. ONC Background
- 1.1.2 B. Interdependencies With Other HITECH Provisions and Relationship to Other Regulatory Requirements and Related Activities
- 1.1.2.1 1. Medicare and Medicaid EHR Incentive Programs Proposed Rule
- 1.1.2.2 2. Health Insurance Portability and Accountability Act of 1996 (HIPAA) Privacy Rule Accounting of Disclosures Regulation
- 1.1.2.3 3. Previous Recognition of Certification Bodies and New Authority Under the HITECH Act
- 1.1.2.4 4. Other HHS Regulatory Actions
- 1.1.3 C. Standards, Implementation Specifications, and Certification Criteria Processes Before and After the HITECH Act
- 1.1.4 D. Future Updates to Standards, Implementation Specifications, and Certification Criteria
- 1.2 II. Overview of the Interim Final Rule
- 1.3 III. Section-By-Section Description of the Interim Final Rule
- 1.3.1 A. Applicability
- 1.3.2 B. Definitions
- 1.3.2.1 1. Definition of Standard
- 1.3.2.2 2. Definition of Implementation Specification
- 1.3.2.3 3. Definition of Certification Criteria
- 1.3.2.4 4. Definition of Qualified Electronic Health Record (EHR)
- 1.3.2.5 5. Definition of EHR Module
- 1.3.2.6 6. Definition of Complete EHR
- 1.3.2.7 7. Definition of Certified EHR Technology
- 1.3.2.8 8. Definition of Disclosure
- 1.3.3 C. Initial Set of Standards, Implementation Specifications, and Certification Criteria
- 1.3.3.1 1. Adopted Certification Criteria
- 1.3.3.2 2. Adopted Standards
- 1.3.3.2.1 a. Transport Standards
- 1.3.3.2.2 b. Content Exchange and Vocabulary Standards
- 1.3.3.2.2.1 i. Patient Summary Record
- 1.3.3.2.2.2 ii. Drug Formulary Check
- 1.3.3.2.2.3 iii. Electronic Prescribing
- 1.3.3.2.2.4 iv. Administrative Transactions
- 1.3.3.2.2.5 v. Quality Reporting
- 1.3.3.2.2.6 vi. Submission of Lab Results to Public Health Agencies
- 1.3.3.2.2.7 vii. Submission to Public Health Agencies for Surveillance or Reporting
- 1.3.3.2.2.8 viii. Submission to Immunization Registries
- 1.3.3.2.2.9 ix. Table 2A
- 1.3.3.2.3 c. Privacy and Security Standards
- 1.3.3.3 3. Adopted Implementation Specifications
- 1.3.3.4 4. Additional Considerations, Clarifications, and Requests for Public Comments
- 1.4 IV. Collection of Information Requirements
- 1.5 V. Regulatory Impact Analysis
- 1.1 I. Background
Table of Contents
I. Background
A. ONC Background
B. Interdependencies With Other HITECH Provisions and Relationship to Other Regulatory Requirements and Related Activities
B. Interdependencies With Other HITECH Provisions and Relationship to Other Regulatory Requirements and Related Activities
The HITECH Act creates multiple interdependencies between this interim final rule and other regulatory requirements, processes, and programs.
1. Medicare and Medicaid EHR Incentive Programs Proposed Rule
2. Health Insurance Portability and Accountability Act of 1996 (HIPAA) Privacy Rule Accounting of Disclosures Regulation
3. Previous Recognition of Certification Bodies and New Authority Under the HITECH Act
4. Other HHS Regulatory Actions
Other HHS Regulatory Actions
