1. Medical History: Detailed medical history section when relevant for complex procedures or ongoing treatments

2. Interpreter Declaration: Required when consent discussions are conducted through an interpreter

3. Research Participation: Additional consent for participation in medical research or clinical trials

4. Photography Consent: Permission for medical photography or recording for documentation or educational purposes

5. Blood Product Refusal: Specific section for patients refusing blood products for religious or personal reasons

6. Specific Procedure Risks: Detailed risks specific to complex procedures or treatments

7. Teaching Facility Disclosure: Required for teaching hospitals where students/residents may be involved in care

1. Schedule A - Procedure Details: Detailed technical description of the medical procedure or treatment plan

2. Schedule B - Risk Disclosure: Comprehensive list of potential risks and complications specific to the treatment

3. Schedule C - Cost Breakdown: Detailed breakdown of expected costs and financial obligations

4. Schedule D - Post-Treatment Care: Instructions for post-treatment care and follow-up requirements

5. Appendix 1 - Medical Terms Glossary: Definitions of medical terms used in the consent form

6. Appendix 2 - Patient Rights Charter: Complete charter of patient rights and responsibilities

7. Appendix 3 - Emergency Protocols: Emergency procedures and contact information for adverse events