The Regulations on Drug Supervision and Administration in Medical Institutions (Trial) was issued on Oct.11, 2011. It aims to strengthen the drug supervision and management of medical institutions, improve the drug quality assurance system, strengthen the drug quality awareness of medical institutions, and ensure the safety of drug use by the people, which includes:
1. General Provisions
2. Drug Purchase and Storage
3. Drug Dispensing and Use
4. Supervision and Inspection
5. Legal Responsibility
6. Supplementary Provisions