Part 113 - Medical Cannabis
- Section 113.1 - Definitions
- Section 113.2 - Practitioner Eligibility
- Section 113.3 - Practitioner Issuance of Certification
- Section 113.4 - Registration Filing Exemptions for Certified Patients and Designated Caregivers
- Section 113.5 - Designated Caregiver Registration
- Section 113.6 - Application for Initial Registration as a Registered Organization
- Section 113.7 - Consideration of Registered Organization Applications
- Section 113.8 - Applications for Renewal of Registration as Registered Organization
- Section 113.9 - Registrations Non-transferable
- Section 113.10 - Failure to Operate
- Section 113.11 - Registered Organizations; General Requirements
- Section 113.12 - Manufacturing Requirements for Medical Cannabis Products
- Section 113.13 - Requirements for Dispensing Sites
- Section 113.14 - Security Requirements for Manufacturing and Dispensing Sites
- Section 113.15 - Laboratory Testing Requirements for Medical Cannabis
- Section 113.16 - Pricing
- Section 113.17 - Medical Cannabis Marketing and Advertising
- Section 113.18 - Reporting Dispensed Medical Cannabis Products
- Section 113.19 - Prohibition on the use of Medical Cannabis Products in Certain Places
- Section 113.20 - Reporting Requirements for Registered Practitioners, Certified Patients and Designated Caregivers
- Section 113.21 - Proper Disposal of Medical Cannabis Products by Certified Patients or Designated Caregivers
- Section 113.22 - General Prohibitions
- Section 113.23 - Practitioner Prohibitions
- Section 113.24 - Designated Caregiver Prohibitions and Protections
- Section 113.25 - Registered Organizations; Disposal of Medical Cannabis
- Section 113.26 - Energy and Environmental Standards and Regulations
- Section 113.27 - Registered Organizations; Inspections and Audits
- Section 113.28 - Referenced Material