Confidentiality rules overlap
42 CFR Part 2, HIPAA, HITECH and state health-information requirements can create different duties for records, notices, consent and disclosure.
Monitor the federal, state, licensing, confidentiality, payer, accreditation and controlled-substance sources your organization selects. When something changes, RegWatch helps your team understand what changed, what may be affected and what to review next.
Requirements may come from federal privacy and treatment-program rules, state licensing agencies, payer programs, controlled-substance authorities and accreditation bodies. RegWatch brings the selected sources into a consistent monitoring and review process.
42 CFR Part 2, HIPAA, HITECH and state health-information requirements can create different duties for records, notices, consent and disclosure.
Outpatient, residential, withdrawal-management and opioid treatment programs may need different watchlists for each location and service model.
SAMHSA, DEA, state agencies and professional boards may publish changes affecting medication treatment, prescribing, dispensing and telehealth workflows.
Patient notices, consent forms, clinical procedures, medication controls and incident-response materials may require review when selected sources change.
Select the jurisdictions and requirements that matter to your services. Expand coverage as facilities, payer relationships, medications and operating models change.
Selected 42 CFR Part 2, HIPAA, HITECH and state health-information sources involving patient records, notices, consent, disclosure and security.
Selected 42 CFR Part 8, SAMHSA certification, accreditation and operational materials relevant to opioid treatment programs.
Selected DEA, federal and state sources involving prescribing, dispensing, recordkeeping, medication controls and telemedicine requirements.
State substance use agencies, facility licensing requirements, professional boards, program manuals and location-specific notices.
Selected CMS, Medicare, state Medicaid and payer-program materials involving participation, coverage, documentation and provider operations.
Selected accreditation standards, workplace safety, emergency preparedness, privacy and cybersecurity guidance relevant to treatment operations.
Monitor availability and applicability vary by source, jurisdiction, program type and organization. Your team chooses the watchlist it wants RegWatch to follow.
Select your monitors, receive organized change intelligence and optionally connect policies for gap assessment.
Choose the confidentiality, treatment-program, licensing, payer, accreditation and controlled-substance sources your organization wants to follow.
See what changed, important dates, affected requirements, source links and suggested review areas.
Upload and assign patient-privacy, consent, clinical, medication, safety or operational policies to the selected monitors they support.
Review potential policy gaps, ownership, next steps, review activity and supporting evidence in a consistent workflow.
RegWatch follows the rule, bulletin, manual, guidance or licensing source your team selects.
The update is captured, summarized and organized so reviewers can focus on what changed.
Your team receives a focused review package instead of another unstructured alert.
RegWatch can support organizations with different facility types, medications, payer relationships and jurisdictional requirements—without forcing every program into the same watchlist.
Create your free monitoring accountReduce repeated searches across federal, state, licensing, payer and accreditation websites.
Give owners the source, dates, affected topics and review context in one place.
Connect selected requirements with the patient-privacy, clinical and operational policies your team relies on.
Keep updates, assessments, ownership, review activity and supporting evidence organized.
Start with regulatory monitoring, then add policy assessment workflows when your team is ready.
Request a DemoOrganizations can select from available federal, state and local sources, including 42 CFR Part 2, HIPAA and HITECH materials, 42 CFR Part 8 and SAMHSA materials for opioid treatment programs, selected DEA sources, CMS and Medicaid materials, licensing authorities, accreditation requirements, workplace safety guidance and cybersecurity sources. Available coverage depends on the selected monitors and sources.
Yes. You can use RegWatch for regulatory monitoring and organized change summaries without uploading policies. Policy uploads are optional and support policy assessment workflows when useful.
Yes. Your watchlist can be organized around the jurisdictions, facilities, program types, medications and payer relationships your organization wants to review. Your team determines which requirements apply.
You can assign uploaded patient-privacy, consent, clinical, medication, safety or operational policies to selected monitors. When those sources change, RegWatch can identify areas that may require review, clarification or remediation.
No. RegWatch provides regulatory intelligence and workflow support. Your organization remains responsible for determining applicability and obtaining legal, clinical or other professional advice where needed.
Get a free RegWatch account and begin building a monitoring watchlist around your programs, locations and selected requirements.