MEDITECH Regulatory

Welcome to MEDITECH's Regulatory Page. Here you will find valuable information, tools, resources, and documentation related to various program requirements.

Regulatory Bulletin Board

Bulletin Board

USCDI, Information Sharing, ASTP Certification Resources & More

Promoting Interoperability (PI) Program

PI FAQs

PI Audit Guides

Certification

PI Presentations

Eligible Hospitals PI Best Practices
Expanse    6.1    6.0    Client/Server    MAGIC

Quality Payment Program (QPP)

QPP FAQs

MIPS Audit Guides

Certification

MIPS Presentations

Eligible Clinicians MIPS Best Practices
Expanse    6.1   6.0   Client/Server   MAGIC

Oncology MACRA/MIPS Best Practices
Expanse 2.2   Expanse 2.1   6.1  Client/Server

Primary Care First (PCF) Resources

Inpatient Quality Reporting (IQR) Program

IQR Resource

National Committee for Quality Assurance (NCQA) Resources

Healthcare Effectiveness Data and Information Set (HEDIS)

Patient-Centered Medical Home/Patient-Centered Specialty Practice (PCMH/PCSP)

Social Determinants of Health (SDOH) Resources

SDOH Resource

Outpatient Quality Reporting (OQR) Program

OQR Resource

Inpatient Rehabilitation Facility (IRF) Quality Reporting Program (QRP)

Minimum Data Set (MDS) Resources

Home Care Resources

Home Care Resource

Government & Industry: Federal and State

ADT Notifications

Appropriate Use Criteria (AUC)

Hospital Respiratory Data (HRD) Resources

EHR Data in Clinical Investigations

Electronic Records & Signatures

FDA

HIPAA

The Joint Commission

Price Transparency

Regulatory Reporting Programs Informational Guide

State Regulations

ISO 9001: 2015 Certification

ISO 27001 Certification

MEDITECH Canada

Canadian Regulatory

Update Files & Grouper

APC Files

Archived ICD-10 Resources

Canadian Files

Grouper Files

Risk Adjustment Model Files

Quality Vantage

Quality Vantage Resource

Contact Us

For information or questions regarding this content, please send a message to MEDITECH's

Regulatory Mailbox