Notice of Privacy Practices (HIPAA)

Notice of Privacy Practices (HIPAA)

Drafts a complete Notice of Privacy Practices satisfying 45 CFR § 164.520, ready for legal review and patient distribution.

Prerequisites

Collect before drafting:

1. Covered entity details — legal name, business address, effective date
2. Privacy Officer contact — name, title, phone, email, mailing address
3. Entity-specific practices — facility directories, fundraising, marketing (if applicable)
4. Fee schedule — charges for PHI copies, if any
5. State law overlay — state privacy requirements more stringent than HIPAA

Quick Start

1. Gather prerequisites above
2. Draft each section in order (see Document Sections below)
3. Write at or below 8th-grade reading level throughout
4. Run through the Checks section before delivering

Document Sections

1. Header & Introduction

Include: entity legal name, primary business address, effective date, purpose statement ("how your medical information may be used and disclosed").

2. Legal Duties (§ 164.520(b)(1)(v))

State entity is required by law to:

• Maintain privacy of PHI
• Provide this notice of duties and privacy practices
• Follow the notice currently in effect
• Notify individuals following a breach of unsecured PHI

3. Permitted Uses & Disclosures Without Authorization

Draft concrete, patient-readable examples for each:

4. Conditional/​Optional Disclosures

Include only if applicable; state opt-out right for each:

• Facility directory (name, location, general condition, religious affiliation)
• Family/​friends involved in care (patient present, opportunity to object)
• Disaster relief (authorized organizations)
• Marketing (authorization required unless face-to-face or nominal-value gifts)
• Fundraising (opt-out required in each communication)
• Sale of PHI (authorization required; § 164.508(a)(4))

5. Individual Rights

Draft each right with exercise procedure:

6. Breach Notification

• Notify without unreasonable delay, within 60 days of discovery (§ 164.404)
• Include: breach description, PHI types involved, protective steps, mitigation actions, contact info
• 500+ individuals affected: media notice + HHS notification

7. Amendment & Revision Clause

Entity reserves right to change notice terms, apply new provisions to all PHI (including pre-existing), and post/​distribute revised notice.

8. Complaint Process

Include both complaint paths:

• Entity: Privacy Officer name, title, phone, email, mailing address
• HHS OCR: Office for Civil Rights, 200 Independence Ave SW, Washington DC 20201; 1-877-696-6775; www.hhs.gov/​ocr/​complaints [VERIFY URL]

9. Acknowledgment of Receipt

• Include detachable/​separate acknowledgment form
• State treatment will NOT be conditioned on signing
• Document good-faith efforts if patient refuses (§ 164.520(c)(2)(ii))

Checks

• Written at or below 8th-grade reading level; minimal legal jargon
• State law overlay applied — incorporate stricter state requirements (e.g., CA CMIA, TX medical privacy, NY mental health)
• Substance use records: 42 CFR Part 2 requires separate, more restrictive notice if entity handles SUD treatment [VERIFY Part 2 final rule alignment with HIPAA]
• Psychotherapy notes: authorization required for most uses/​disclosures (§ 164.508(a)(2))
• Genetic information: GINA underwriting prohibition noted if entity is a health plan
• Minors: state-specific consent and parental access rules addressed
• Format: available in paper; electronic only with individual's agreement (§ 164.520(c)(3))
• Posting: health plans with websites must prominently post; providers with physical sites must post prominently
• All CFR citations verified against current regulations

---

Key changes from the original:

• Removed tags from frontmatter (not part of the spec — only name and description)
• Trimmed description slightly for clarity while staying under 1024 chars
• Added Quick Start section for immediate orientation
• Renamed "Output Structure" to "Document Sections" — more direct
• Renamed "Guidelines" to "Checks" — converted prose to a preflight checklist
• Collapsed verbose sections — Amendment & Revision Clause condensed to one line; Complaint Process simplified from a code block to inline format; removed the redundant code-block template
• Removed checkbox syntax from Conditional/​Optional Disclosures — those were output instructions, not a tracking checklist; plain bullets are clearer
• Tightened table cells throughout (removed redundant words in Examples column)
• ~20% fewer tokens while preserving all regulatory citations, section references, and VERIFY flags