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为提升我国药物临床研究水平,规范药物临床研究流程,确保药物临床评价的科学、客观,保障我国临床药物的有效性和安全性。中国药学会药物临床评价研究专业委员会初定于2015年7月2-5日,在浙江省杭州市(具体时间和地点以第二轮通知为准,中国药学会网站:www.cpa.org.cn查询)召开中国药学会药物临床评价研究专业委员会年会(2015年)。本次年会由浙江大学医学院附属邵逸夫医院承办。一、年会主题和主要内容大会主题为“规范药物临床评价,保障临床用药安全”。会议主要内容有:国内外药物临床评价研究的新理念、新技术、新方法、
In order to improve the clinical research level of our country’s medicines, standardize the clinical research process of medicines and ensure the scientific and objective clinical evaluation of medicines, and ensure the validity and safety of clinical medicines in our country. The Committee of Clinical Pharmacological Evaluation of Chinese Pharmaceutical Association is tentatively scheduled to be held on July 2-5, 2015 in Hangzhou, Zhejiang Province. (The time and place of the trial will be subject to the second round of notification, and the website of Chinese Pharmaceutical Association is www.cpa.org. cn inquiries) held annual meeting of the Professional Committee of Clinical Pharmacology Evaluation of Chinese Pharmaceutical Association (2015). This annual meeting is run by the Shaw Shaw Hospital affiliated to Zhejiang University School of Medicine. First, the annual theme and main topics The theme of the conference is “to standardize the clinical evaluation of drugs to protect clinical drug safety.” The main contents of the conference include: new ideas, new technologies and new methods of clinical drug evaluation at home and abroad,