Article 1 In order to strengthen the standardized management of prescription preparation, dispensing, use and preservation, improve prescription quality, promote rational drug use, and ensure the safety of patients' drug use, these Measures are formulated in accordance with the Law on Medical Practitioners, the Drug Administration Law, the Regulations on the Administration of Medical Institutions and other relevant laws and regulations.

Article 2 These Measures shall apply to the corresponding institutions and personnel that distribute, examine, adjust and keep prescriptions.

Article 3 Prescription refers to the medical documents issued by registered medical practitioners and assistant medical practitioners (hereinafter referred to as doctors) for patients in the process of diagnosis and treatment, which are examined, prepared and checked by pharmaceutical professional and technical personnel as the vouchers for dispensing drugs.

Article 4 The sale, deployment and use of prescription drugs must be based on a doctor's prescription.

Doctors' prescriptions and pharmacy professionals' prescriptions should follow the principles of safety, effectiveness and economy, and pay attention to protecting patients' privacy.

Article 5 A registered doctor shall obtain the corresponding prescription right in the practice place.

A prescription issued by a registered assistant practicing physician shall be valid only after the signature or seal of the practicing physician at the place where he practices.

Registered practicing assistant doctors practice in medical, preventive and health care institutions in townships, nationality townships and towns, and obtain corresponding prescription rights in registered practice places.

Prescriptions made by doctors during the probation period shall be examined by medical practitioners who have the right to prescribe in their medical, preventive and health care institutions, and shall be valid only after they are signed or stamped with special seals. Doctors must sign and keep samples in registered medical, preventive and health care institutions, and sign for the record before prescribing.

When a doctor is ordered to suspend his practice, be ordered to leave his post for training, be cancelled or revoke his practice certificate, his prescription right will be revoked.

Article 6 Doctors should prescribe according to the medical treatment, prevention, health care needs, indications, pharmacological effects, usage, dosage, contraindications, adverse reactions and precautions in the medical specifications and drug instructions. The prescriptions of narcotic drugs, psychotropic drugs, toxic drugs for medical use and radioactive drugs must strictly abide by the provisions of relevant laws, regulations and rules.

Article 7 This prescription is effective from the date of issuance. If it is necessary to extend the validity period under special circumstances, the prescriber shall indicate the validity period, but the longest validity period shall not exceed 3 days.

Article 8 The prescription format consists of three parts:

(1) Foreword: including the name of medical, preventive and health care institutions, prescription number, charging standard, patient's name, gender, age, outpatient or inpatient medical record number, department or ward and bed number, clinical diagnosis, date of issuance, etc. , and can increase the professional needs of the project.

(2) Text: marked with Rp or R (abbreviation of Latin prescription "Please take"), indicating the name, specification, quantity, usage and dosage of the drug.

(3) Remarks: the signature and/or special seal of the doctor, the signature of the pharmaceutical professional technicians who examine, allocate, check and distribute the drugs.