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1. Title and Document Identification: Clear identification of the document as a Patient Consent Form for Case Report, including institution name and form version/date
2. Patient Information: Patient's name, date of birth, contact details, and medical record number (while noting that this may be anonymized in the actual case report)
3. Healthcare Provider Information: Name and contact details of the primary healthcare provider/researcher responsible for the case report
4. Purpose of the Case Report: Clear explanation of why the case report is being written and its intended use in medical literature
5. Information to be Published: Specific details about what medical information will be included in the case report
6. Confidentiality Statement: Explanation of how patient's privacy will be protected and what identifying information will be removed/modified
7. Rights Statement: Clear outline of patient's rights, including the right to withdraw consent
8. Consent Declaration: Formal statement of consent with specific permissions being granted
9. Signatures: Space for patient (or legal representative) signature, date, and witness signature if required
1. Interpreter Declaration: Required when the patient's primary language is not English or when an interpreter is used
2. Legal Representative Authorization: Required when the patient is unable to provide consent themselves
3. Photography/Images Consent: Required when the case report will include photos, x-rays, or other images of the patient
4. Future Use Permission: Optional section for consent to use the case report in future medical education or research
5. Financial Disclosure: Required when there are any financial implications or compensation related to the case report
6. Publication Details: Optional section specifying intended publication venues or specific journals
1. Description of Case Report: Detailed outline of the medical condition or procedure that will be described in the case report
2. Image Schedule: List and descriptions of any images or medical records that will be included in the publication
3. Privacy Protection Measures: Detailed description of steps taken to protect patient privacy and confidentiality
4. Patient Rights Information Sheet: Detailed information about patient rights under New Zealand law regarding medical information and privacy
5. Withdrawal Process Guide: Detailed information about how to withdraw consent and the implications of withdrawal
Personal Information
Health Information
Consent
Publication
Healthcare Provider
Medical Journal
Anonymisation
Confidential Information
Clinical Images
Medical Records
Withdrawal of Consent
Legal Representative
Principal Investigator
Research Institution
Protected Health Information
Identifying Information
Academic Use
Educational Purpose
Medical Literature
Privacy Protection Measures
Professional Audience
Data Protection
Publication Rights
Authorized Recipients
Privacy
Confidentiality
Data Protection
Publication Rights
Patient Rights
Withdrawal Rights
Information Use
Image Rights
Medical Records Access
Third Party Disclosure
Anonymity Protection
Duration and Survival
Liability and Indemnification
Governing Law
Dispute Resolution
Amendment and Modification
Severability
Entire Agreement
Acknowledgment and Declaration
Healthcare
Medical Research
Academic Medicine
Clinical Practice
Medical Education
Medical Publishing
Healthcare Administration
Medical Ethics
Legal
Compliance
Medical Records
Research
Clinical Operations
Ethics Committee
Privacy Office
Medical Affairs
Publication
Patient Services
Quality Assurance
Medical Doctor
Clinical Researcher
Research Nurse
Medical Ethics Officer
Privacy Officer
Healthcare Administrator
Clinical Director
Medical Writer
Research Coordinator
Legal Counsel
Compliance Officer
Medical Records Manager
Research Ethics Committee Member
Medical Publisher
Academic Medical Professor
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