(As of 98th Standing Committee of the People's Government of the Wider Self-Government Zone, held on 31 December 2011, the consideration of the adoption of the Decree No. 74 of 19 January 2012 of the People's Government Order No. 74 of 19 January 2012 for the Greater Self-Government Zone, which came into force on 1 April 2012.

Chapter I General

In order to strengthen the management of medical institutions, regulate the operation of health-care institutions and promote the development of health-care services, and develop this approach in line with the provisions of the State Department's Medical Institutions Management Regulations and relevant legislation.

Article 2

The medical institutions described in this approach include hospitals at all levels, maternal and child health, community health services centres (stays, hospitals, hospitals), nursing homes, specialist illness control boards (as well as clinics, clinics, nursing homes (stays), medical services, health care, first-centres, clinical testing centres.

Disease prevention controls, national sanitary quarantine, medical scientific research and teaching, medicine, family planning services operate outside the scope of their operations, with the approval of appropriate categories of medical institutions by law.

Article 3. The management of medical institutions is decentralized and sector-wide.

Article IV. The Government of the above-mentioned population should incorporate health-care institutions in the overall planning of local economic and social development and urban-rural-building, integrate and optimize the allocation of medical resources; adhere to public health institutions as the lead, non-public health institutions and complement non-profit medical institutions; implement the health agency government subsidy, compensation policy, and establish and improve the health-care system for rural and urban residents.

Article 5 The authorities are responsible for the supervision of medical institutions.

Chapter II

The Government's health administration should be based on the population, the economic situation and medical resources, medical needs, the distribution of existing medical institutions, the preparation or revision of the planning of medical institutions, with the consent of the Government's health administration at the highest level, the approval of implementation by the current people's Government and the publication of the society.

The development or revision of health-care institutions should be synchronized with the overall planning for rural and urban development.

Article 7

The new establishment of non-public medical institutions in urban municipalities has been established by public competition.

Article 8 shall require the establishment of a medical institution to:

(i) In line with the planning of medical institutions;

(ii) The basic standards of the same kind of medical institutions, such as the organization, staffing, equipment configuration, etc., consistent with national standards;

(iii) The establishment of an independent civil responsibility;

(iv) Provide a letter of credit to meet the total investment;

(v) The reasonableness of the medical waste disposal programme;

(vi) Other conditions under the law, regulations.

Article 9 requests for the establishment of an individual clinic and, in addition to the conditions set out in article 8 of this approach, shall also have the following conditions:

(i) himself acquires the qualifications of a medical doctor, who is registered in the same profession for more than five years;

(ii) A medical, secondary or oral category.

Article 10 requires the establishment of medical institutions and shall apply to the health administration with the authorization authority and submit written material in accordance with the provisions.

Article 11. The health administration shall establish the approval of medical institutions in accordance with the following terms:

(i) Level 3 hospitals and gynaecologists, specialised diseases control boards (see para.

(ii) Sub-primary hospitals, tiers and gynaecology, specialist hospitals, mid-medical hospitals (including secondary medical combinations, national health), 100 rehabilitation hospitals, nursing homes, nursing homes and medical clinics (clinics) etc., are approved by the district-level people's Government's health administration after clearance of the health administration;

(iii) The commune of the town, the Centre for Community Health Services (at the station), the establishment of 100 dissidents and other medical institutions with no-beds, which are approved by the Government of Health at the district level;

(iv) The establishment of joint ventures and cooperative medical institutions, which are reviewed by the Government's Health Administration in the districts, and the approval of the Government's Health Administration and the Commercial Administration of the self-government sector;

(v) Hong Kong, Macao medical service providers have a personal clinic in the self-government area, which is approved by the Government's Health Administration of the People's Government of the Autonomous Region following the review of the Government's health administration.

The establishment of public health institutions should be approved by the health administration in conjunction with government agencies.

Article 12 Prior to the nuclear launch of the instrument of ratification of the establishment of a medical institution, the health administration should be presented to society for a period of five working days. The presentations include the names, categories, tiers, addresses, treatment subjects, beds, names of applicants and compliance with local medical institutions planning.

Article 13

(i) Clinic, hygienic (at stations, hospitals, hospitals), health-care centres, medical services, referrals and other undesirable medical institutions for a year;

(ii) Two years for medical institutions, clinical test centres, medical tests;

(iii) More than 100 beded medical institutions are three years.

More than an effective period of non-application of the executive branch, the instrument of ratification of the establishment of a medical institution has no effect.

Article XIV Changes in the category, level or address approved by medical institutions should be re-established.

Medical institutions need to establish branches of medical institutions, and procedures should be conducted in accordance with the provisions of the new medical establishment.

Chapter III Registration and school tests

Article 15. Medical institutions shall apply to the authorized health administration to register and receive a licence for the operation of the medical institutions, after completing the matters approved by the establishment of a medical institution.

The establishment of a drug-recovery medical institution or a medical agency for the treatment of poisoning, as well as the establishment of a medium-sized joint venture and cooperation medical facility, should apply to the Government's health administration in the area where it is located; Hong Kong, Macao medical service providers have an independent clinic and should be registered with the Government's health administration in the area.

Article 16 shall submit the following material:

(i) Applications for registration in the business;

(ii) The instrument of ratification of medical institutions;

(iii) Housing property certificates or proof of use;

(iv) The construction design or operation of a slogan;

(v) Receives, asset assessment reports;

(vi) List of statutory representatives or principal heads of departments;

(vii) Registration of applications by doctors, nurses;

(viii) List of major equipment;

(ix) Programme for the allocation of drug supply facilities and disposal of medical wastes;

(x) Management systems and technical operating protocols.

Article 17 The health administration should conduct field inspections of medical institutions applying for the administration of justice within 45 days of the date of receipt, on a case-by-case basis. In accordance with conditions, a licence for the operation of a medical institution is granted; it is not in accordance with the conditions and a written justification.

The Medical Agency's Execution Licence and its copies are produced by the Government's Health Administration at the district level, in accordance with the pattern established by the Ministry of Health.

The name of the medical institution may be used after the registration is approved by the health administration.

Medical institutions are allowed to register only one category and one name. There is a need to use two names, which should be approved by the health administration and to identify the first name as registration name.

Article 19

(i) A State, society or public interest;

(ii) Violations of the legitimate rights and interests of others;

(iii) The composition of the delegation of the Chinese language;

(iv) Designation of medical instruments, medicines, medical products;

(v) Advocacy or implied the effectiveness of the treatment;

(vi) In addition to the scope of the registered medical treatment subject;

(vii) In the name of men, male or female;

(viii) The name identified by a non-sixed relationship unit or by a non-resident medical agency;

(ix) To be converted into administrative areas (except the provisions of article 20 of the Government's medical institutions and this approach).

The name of the medical institution contains the words “wide wide” and the regional name of the cross-city district administration, or the designation as a generic name of the medical institution (other than the Centre's Health, the Community Health Centre), which is approved by the Government of the Autonomous Region.

The name of the medical body includes “China”, “National”, “China”, “National”, “ASEAN”, “international” and foreign States (zone), international organizations should be approved by the Health Administration of the State Department of State, upon review by the Government of the self-government.

Article 21 Changes in names, statutory representations or principals, operational nature, beds (dental chairs) and medical subjects should apply to the former registered health administration for registration procedures.

Article 22 provides for a regular school test system. Medical institutions shall apply to the registry in accordance with the following school time period:

(i) More than 100 integrated hospitals, mid-care (including secondary medical combinations, national health) hospitals and specialist hospitals, rehabilitation hospitals, nursing homes, maternity and child health institutions, emergency centres, clinical testing centres, medical tests and specialist disease prevention institutions for a period of three years, and other medical institutions have been recruited for one year;

(ii) The number of schools for joint venture cooperation medical institutions is one year;

(iii) The next period of school inspection of qualified medical institutions after probationary school tests is one year.

Article 23. Medical institutions shall apply to the registration authorities within three months prior to the expiration of the school inspection and submit the following materials:

(i) The application for the accreditation of medical institutions;

(ii) The Licence of the Medical Institutions and their copies;

(iii) Report on the functioning of the school cycle;

(iv) Other material provided by the Government's Health Administration in the self-government area.

In addition to the submission of the materials provided for in the above-mentioned paragraph, an individual clinic shall also submit a recent physical health certificate to the practitioners.

Article 24 shall complete the review of school tests within 30 days of the date of receipt of the application for admission to school, with the conclusion of school tests. The findings of school tests are divided into prequalification and probationary school tests. The probationary inspection should determine the duration of the probationary school and the probationary period is between 1 and 6 months.

During the probationary period, no-bed medical institution shall be allowed to carry out medical treatment activities, and the medical institutions set up are not allowed to carry out induction operations and to receive new patients, with the exception of first aid.

Article 25 Medical institutions have one of the following cases, and registration authorities may write their licenses for the operation of medical institutions:

(i) Curriculum expires and not to apply for school tests for more than 30 days;

(ii) The re-entry test after the suspension of school tests remains unqualified;

(iii) There shall be no justification for the termination of medical activities or for the suspension of more than one year;

(iv) Other cases to be cancelled by law, legislation and regulations.

The registration authority may write the subject of the medical treatment to the extent that the school was found to have no medical treatment.

Chapter IV

Article 26 does not obtain a licence for the operation of the medical institutions.

Medical institutions should conduct diagnostic activities in accordance with the licensing of the medical institutions. The Medical Agency's Procedural Licence shall be charged with a noticeable place.

Article 27 Medical institutions may not be allowed to sell, transfer, rent or borrow the name of the Medical Agency's ruling and the medical agency; they shall not be granted a medical place, contracted to other agencies or persons for medical treatment in the name of the medical institution.

The second eighty-eight medical institutions should have a system of health technicians, facilities equipment and quality control adapted to them and adhere to technical management norms.

Medical institutions may not use non-hygienic technicians to engage in health-care technology, and health technicians may not be organized for medical activities other than their own profession.

The twenty-ninth medical institutions should strengthen the management of drug clinical applications, implement national basic drug systems, provide for the availability and use of basic drugs, and use of narcotic drugs, toxic medicines, mental medicines and radioactive drugs should be in line with national provisions.

Medical institutions are not equipped with registered medical doctors, nurses and pharmacological technics determined by law, without the corresponding first-aid medicines, and are not allowed to carry out static pharmaceutical operations.

Article 33 Medical institutions should strengthen the management of infection, strictly the implementation of the sterilization system, scientific and effective measures to address sewage and medical wastes and to prevent and control hospital infection.

Article 31 Medical institutions should fulfil their public health services and emergency relief obligations under the law, assume the prevention of infectious diseases in the area of medical treatment and responsibility for treatment; identify epidemics should be reported in a timely manner and take effective measures to control the spread of epidemics; and in cases of sudden public events or emergency relief needs, medical institutions and their medical personnel should be subject to the release of the health administration.

Medical institutions and their medical personnel should participate in the work of the Health Administration in the area of oral support and health services at the grass-roots level.

Article 32 Medical institutions should implement the health-care fee policy established by the State and the self-governing area, without unauthorized increases in fees projects or raising the fee rate.

Article 33 Medical institutions should properly preserve the medical instruments and maintain their true, completeness, without unauthorized modification, alteration, concealment, falsification and early destruction.

The medical agency's bill of fees, the accounts of income and expenditure, medical certificates of origin should be maintained for more than 15 years and the hospitalization period for more than 30 years. The duration of the maintenance of the opening-up is carried out in accordance with the relevant provisions of the State.

Medical institutions may not give false test reports and medical certificates such as medical treatment, birth and death.

The publication of medical advertisements by medical institutions should be subject to a medical examination issued by the Government of the People's Government of the self-government in the area of health administration, which should not exceed the scope of the review certificate.

In cases where medical institutions perform operations, special inspections or special treatments, information on medical risks, alternative health programmes, etc., should be provided to patients in a timely manner, with their written consent, and if it is not appropriate to explain to the patient, the written consent of the patient's close relatives or guardians should be obtained. However, due to the need to stifle life-threatening patients, the patient or his close relatives, guardians agree, and the medical agency heads or authorized heads may immediately implement the corresponding medical measures.

No activities such as genetic diagnosis, prenatal diagnosis, termination of pregnancy and stereotype gender identification and other family planning operations are carried out without the approval of medical institutions.

Oversight inspection

The Government's health administration in article 37 should strengthen the supervision of the health administration of the lower-level people, and correct in a timely manner violations in medical institutions for the approval, registration, school tests and law enforcement inspections.

Article 338. Health administration law enforcement officers carry out health surveillance inspections of medical institutions and perform the following duties under the law:

(i) On-site inspection of relevant places of medical treatment;

(ii) To ask the parties to investigate the relevant situation;

(iii) Access, adaptation of relevant information;

(iv) Health in cases where evidence may be lost or otherwise difficult to obtain.

The executive heads agreed that the items relating to therapeutic sites could be registered first. Medical institutions and their staff should cooperate without denying, concealing and concealing them.

Article 39, the supervision of medical institutions by health administrative law enforcement officials, by law, should be recorded in the monitoring and treatment of the results. The inspection records should serve as an important basis for the testing, evaluation or case handling of medical institutions.

Article 40 Medical institutions should establish a system of self-assessment of the quality of medical services, reproduces the problems identified in the self-assessment and submit a self-assessment report to the registry in January of each year.

Medical agencies do not submit annual reports on the quality of medical services self-execution or the report on the performance of the school cycle, and the registration authorities may redeploy their probationary examinations.

Article 40. The Government's health administration is responsible for organizing the evaluation board of the current level of health-care institutions, and making evaluation findings in accordance with the evaluation methodology and standards of the Government of the People's Government of the National and Self-Governmental Region in relation to health-care institutions.

The evaluation findings serve as an important basis for the assessment of the level of medical institutions and for the testing of schools.

Article 42, medical institutions should establish sound financial management systems and asset management systems to receive oversight in the relevant sectors.

Medical institutions are equipped with large-scale medical equipment, which is subject to the principle of territorialization by medical institutions to the Government's health administration, which is on a case-by-step basis, and can be acquired by the licensor.

Chapter VI Legal responsibility

Article 43, in violation of the provisions of this approach, provides for legal responsibility under the law, legislation and regulations.

In violation of article 22 of this approach, the medical institutions have delayed the inspection of the Medical Agency's Execution Licence Licence, which is subject to a deadline for the Government's health administration at the district level, and the denial of school tests and the release of the Medical Agency's authorization by law.

In violation of article 24, paragraph 2, of the scheme, medical institutions have been able to carry out their own medical treatment activities during the probationary school period, which is being reorganized by the Government's Health Administration at the district level and can be fined by more than 1,000 dollars.

Article 42, in violation of article 26 of this approach, provides that medical treatment activities are not carried out by the Medical Agency's Execution Licence, and that the Government's health administration is responsible for the cessation of the operation, forfeiture of illegal proceeds and medicines, equipment and fines of up to 10,000 dollars.

In violation of article 27 of the scheme, the medical institutions rent the medical facility, contracted other agencies or personnel to carry out medical treatment activities on behalf of this medical institution, with a fine of up to 50,000 dollars for the Government's health administration.

Article 47 medical institutions do not have the conditions set out in article 29, paragraph 2, of this approach, to carry out a staple pharmacies operation, which is being converted by the Government's Health Administration for more than 3,000 dollars at the district level.

In violation of article 36 of this scheme, medical institutions have not been authorized to engage in genetic diagnostics, prenatal diagnosis, termination of pregnancy operations, warnings by the health administration of the Government of the more people at the district level, confiscation of proceeds of conflict and related medicines, medical equipment, and fines of up to $200 million.

Chapter VII

Article 49 of this approach is implemented effective 1 April 2012. The provisional approach to the management of health institutions in the San Francisco self-government area, enacted by the Government of the People's Democratic Party in 2000, was also repealed.