Rule 856 IAC 1-30 - Sterile Pharmaceuticals; Preparation and Dispensing
- Section 856 IAC 1-30-1 - Purpose
- Section 856 IAC 1-30-2 - "Biological safety cabinet" defined
- Section 856 IAC 1-30-3 - "Class 100 environment" defined
- Section 856 IAC 1-30-4 - "Cytotoxic" defined
- Section 856 IAC 1-30-4.1 - "Hazardous" defined
- Section 856 IAC 1-30-4.2 - "ISO" defined
- Section 856 IAC 1-30-4.3 - "NSF" defined
- Section 856 IAC 1-30-4.4 - "Parenteral" defined
- Section 856 IAC 1-30-4.5 - "Positive patient outcome" defined
- Section 856 IAC 1-30-4.6 - "Product quality and characteristics" defined
- Section 856 IAC 1-30-5 - "Qualified pharmacist" defined
- Section 856 IAC 1-30-6 - "Sterile pharmaceutical" defined
- Section 856 IAC 1-30-7 - Policy and procedure manual
- Section 856 IAC 1-30-8 - Physical requirements
- Section 856 IAC 1-30-9 - Personnel
- Section 856 IAC 1-30-10 - Support personnel
- Section 856 IAC 1-30-11 - Staffing
- Section 856 IAC 1-30-12 - Profile or medication record system
- Section 856 IAC 1-30-13 - Labeling
- Section 856 IAC 1-30-14 - Records and reports
- Section 856 IAC 1-30-15 - Disposal of infectious waste
- Section 856 IAC 1-30-16 - Emergency kit
- Section 856 IAC 1-30-17 - Hazardous drugs
- Section 856 IAC 1-30-18 - Quality assurance