Indiana · Regulations
Rule 30 — Sterile Pharmaceuticals; Preparation and Dispensing
24 sections
24 sections
- 856 IAC 1-30-1856 IAC 1-30-1 Purpose
- 856 IAC 1-30-2856 IAC 1-30-2 "Biological safety cabinet" defined
- 856 IAC 1-30-3856 IAC 1-30-3 "Class 100 environment" defined
- 856 IAC 1-30-4856 IAC 1-30-4 "Cytotoxic" defined
- 856 IAC 1-30-4.1856 IAC 1-30-4.1 "Hazardous" defined
- 856 IAC 1-30-4.2856 IAC 1-30-4.2 "ISO" defined
- 856 IAC 1-30-4.3856 IAC 1-30-4.3 "NSF" defined
- 856 IAC 1-30-4.4856 IAC 1-30-4.4 "Parenteral" defined
- 856 IAC 1-30-4.5856 IAC 1-30-4.5 "Positive patient outcome" defined
- 856 IAC 1-30-4.6856 IAC 1-30-4.6 "Product quality and characteristics" defined
- 856 IAC 1-30-5856 IAC 1-30-5 "Qualified pharmacist" defined
- 856 IAC 1-30-6856 IAC 1-30-6 "Sterile pharmaceutical" defined
- 856 IAC 1-30-7856 IAC 1-30-7 Policy and procedure manual
- 856 IAC 1-30-8856 IAC 1-30-8 Physical requirements
- 856 IAC 1-30-9856 IAC 1-30-9 Personnel
- 856 IAC 1-30-10856 IAC 1-30-10 Support personnel
- 856 IAC 1-30-11856 IAC 1-30-11 Staffing
- 856 IAC 1-30-12856 IAC 1-30-12 Profile or medication record system
- 856 IAC 1-30-13856 IAC 1-30-13 Labeling
- 856 IAC 1-30-14856 IAC 1-30-14 Records and reports
- 856 IAC 1-30-15856 IAC 1-30-15 Disposal of infectious waste
- 856 IAC 1-30-16856 IAC 1-30-16 Emergency kit
- 856 IAC 1-30-17856 IAC 1-30-17 Hazardous drugs
- 856 IAC 1-30-18856 IAC 1-30-18 Quality assurance