the post-processing images and dsa were analyzed and evaluated by 2 radiologists at double blinded.

method and evaluation of coronary angiography: using the method of judkins, angiographic results obtained by two experienced cardiac catheterization doctors.

冠脉造影方法及评价：造影结果由两位经验丰富的心导管医师采用Judkins法进行判定。

similarly 3 other pet/ ct doctors interpreted the images semi-quantitatively and visually, and made diagnostic and staging conclusions together.

由3位PET／CT医师采用目测法和半定量法相结合对PET图像、CT图像、PET／CT融合图像进行分析，给出诊断及淋巴结相关分期结论。

methods 35 cases with 43 aneurysms were examined by 3d-tof mra. mri and dsa. images were blindly interpreted by 2 neuroradiologists in order to determine the sensitivities of 3d-tof mra.

方法35例颅内动脉瘤患者同时行3D TOF法MRA、MRI及DSA检查，两名神经放射医师盲法分析图象，研究：3D TOF法MRA诊断动脉瘤的敏感性。

objective: through the enforcement of medical doctor law, management regulatory of medical institutes, and treatment rules of medical accedents, to definite the importance of the obligation for doctors and institutes informing patients know about the consent and selection right of patient.

目的：通过《医师法》、《医疗机构管理条例》和《医疗事故处理条例》的实施，明确了医疗机构及医务人员告知义务和患者知情同意和知情选择的重要性。

methods a classified statistics was made of defects in medical record. by the standards of management regulation of medical institutions, medical practician law, and medical and nursing technical operation routine, to analyse the causes.

方法对病案缺陷进行分类统计，对照《医疗机构管理条例》、《执业医师法》、《医疗护理技术操作常规》规定，分析原因。

viewpoints resulting from a study of medical practitioners act of the prc; aiming to standardize the doctor quality, many countries have carried out the examinations of doctors' qualification.

学习中华人民共和国执业医师法后的几点见解为规范医师执业，多数国家实行医师资格考试制度。

this paper first put forward in the field that compulsory medical liability insurance should be written in medical practitioner act.

本文在业界首次提出将强制参加医疗责任保险写入《执业医师法》。

relevant laws request the medical staff to protect the rights informed consent of patients.

《中华人民共和国执业医师法》、《医疗事故处理条例》等国家法律、法规要求医疗机构及其医务人员在医疗活动中，应当维护患者的知情同意权。

informed consent-patients' right and the legislation

知情同意病人的权利与立法兼谈对《执业医师法》第26、37条的修改

combining with the actual status, some thoughts on studying the drug administration law of the people; s republic of china are given in the aspects of position, functions and legal responsibilities of institutes for drug control in drug supervision and management.

本文结合我国药品检验机构的现状，从药品检验机构的地位、职能、作用及法律责任等方面谈了学习《药品管理法》的体会。

the label requirements, such as the required format, particulars and contents, are of great significance in the implementation of drug administration law, the investigation and seizure of adulterated drugs, and the assurance of safe and effective use of drugs in man.

提出了药品标签的统一的格式、栏目、内容的具体要求，对于全面实施《药品管理法》、查处假劣药品、保证人民用药安全有效有着重要意义。

results& conclusions: the registration and approval of drugs and their patents right protection were legally independent of each other, to which the drug administration law and patent law respectively are appli-cable.

结果与结论：药品注册审批与专利权保护是相对独立的法律关系，分别适用药品管理法和专利法；

some suggestions are offered on the management of drug purchasing in medical units and the revising of drug administrative law.

结合基层药品监督管理工作实际，就医疗机构配用药品的管理和《药品管理法》的修改提出建议。

therefore, the fda of the united states has amended the food and drug act in accordance with the models and thus the natural products of cam are easier to gain market than synthetic products and highly purified monomers.

美国药品和食品管理委员会（FDA）根据这一模式对食物和药品管理法作出了一些修改，使得CAM的天然产品比合成产物或高纯度单体，更容易进入美国市场[3]。

the drug prices must be verified and established by the price administration department according to" price law", "drug administration law".

而药品价格由价格管理部门&国家发改委、物价局根据《价格法》、《药品管理法》进行审核和制定。

the port drug administration shall make a decision of administrative sanctions in accordance with the pharmaceutical administration law and other relevant regulations.

口岸药品监督管理局应当按照《药品管理法》以及有关规定作出行政处理决定。

the inferior medicines referred to in this article mean those inferior pharmaceutical products that fall into the category of inferior medicines in accordance with the regulations of the "law of the prc governing the management of pharmaceutical products".

本条所称劣药，是指依照《中华人民共和国药品管理法》的规定属于劣药的药品。

according to drug administration law of the people's republic of china, drug inspecting result should be provided by the drug testing institution in the penalty notification for deteriorated and contaminated drugs.

根据《药品管理法》，变质或被污染药品按假药论处的处罚通知上必须载明药品质量检验结果。

ex: under/ in accordance with a general rule of the pharmaceutical law, the sponsor and the investigator are responsible for damage resulting from conducting a clinical trial.

例句：根据药品管理法规定，临床试验的赞助者和研究者要对试验所造成的后果负责。

the achievement in the implementation of drug administration law for 13 years in guangdong province are summarized, the problems and their existing reasons are analyzed.

总结广东省贯彻执行《药品管理法》13年来取得的10个方面的主要成效，分析存在问题及原因。