Tuesday, April 12, 2011

全球最長壽的藥廠-陳李濟 發展健康體驗產業

廣藥集團成立陳李濟健康養生研究院

42,廣藥集團振興"大南藥"、推進"大健康"步伐再有標誌性進展。歷經4年多的籌備,廣藥集團"嶺南中醫藥文化體驗館"、"陳李濟健康養生研究院"在陳李濟舊址正式成立。記者瞭解到,廣藥集團陳李濟藥廠是中國四大"百年老店"之一,至今已經有411年歷史,其在20109月正式通過吉尼斯世界紀錄現場認證,成為全球最長壽的藥廠。按照廣藥集團"大南藥、大健康"的總體規劃思路,陳李濟作為最老的品牌,將區別于潘高夀、王老吉、采芝林、白雲山和黃、中一等廣藥旗下的其他企業的品牌文化和發展戰略,重點發展中醫藥健康養生文化及產品。廣藥集團方面表示,發展"大南藥"旨在弘揚具有南藥特色的中醫藥文化,充分利用華南特別是嶺南地區中醫藥發展和應用的良好環境,堅持推動中醫藥的大眾化、科普化進程,以文化帶動產業,最終促進"大南藥"事業的發展。而陳李濟健康養生研究院的成立,就是希望進一步研究、發展中醫藥對人類健康長壽的特有作用,促進中醫藥文化和嶺南特色文化得到更廣泛的普及和弘揚。據悉,陳李濟健康養生研究院著力於以"科技研發中心"為主體開展健康養生系列產品研究;為百姓提供健康管理、健康養生知識諮詢、培訓、體驗為內容的服務;建立健康養生網站,為百姓提供健康養生知識網路聯繫和溝通、交流;廣集民間健康養生秘訣歸納研究,豐富發展健康養生領域。

成都國際醫學城的健康休閒基地PK 台灣國際醫療專區

程京院士呼籲關注中國分子診斷產業的\"工業化\"發展

生物谷  2011-04-13 與會專家認為,政府應該更好的和企業溝通交流,制定合理的政策法規,促進產業健康的發展。第二屆中國分子診斷技術大會第一天的主題是轉化醫學,程京院士說:\"轉化醫學不是簡單的說臨床提出問題,到了實驗室做了結果再回到臨床。我認為少了一個\'\',叫工業化。沒有哪個醫院敢用一個大學實驗室做出來的東西,去給病人出診斷證書,或是去做治療。轉化醫學要離開工業化,肯定是不成立的\"\"中國的診斷工業,像比較新的分子診斷,作為工業界的,一定要高度關注。\"韓德民教授認為\"看病貴、看病難\"是當前很重要的一個問題,解決這個問題,分子診斷的發展可以起到很好的一個作用。分子診斷領域是一個非常新的、具有挑戰性的領域。目前發展還處在起步的階段,希望通過呼籲,可以使政府更加的注重這個行業的發展。成都和重慶政府都非常關注醫學的發展,程京院士介紹道,重慶市長黃奇帆宴請二十幾個工程院院士,黃奇帆市長說,\"如果重慶市拿出幾十個億,做高端分子診斷檢測,我要讓全國,甚至是全世界的一部分地方的人,搞不定的疑難雜症,他得到我重慶來\"。程京院士感慨道:\"  成都和重慶,兩個城市相隔這麼近,都對醫學這麼感興趣,這麼前衛和高瞻遠矚,讓北京、上海這些城市汗顏。\"

分子診斷的產業集群效應及成都國際醫學城發展模式 分子診斷作為醫學檢測的核心領域,產業集群化可以提高其產業的深度和產業鏈的延伸,其產業集群的發展模式已受到政府和業內人士的廣泛關注。 在當天論壇上,來自成都國際醫學城指揮部指揮長何敏介紹道,成都國際醫學城致力打造全國知名的健康休閒基地,以成都國際醫學城設計的系統的健康產業集群為例,它是以高端治療為核心,向產業鏈兩端發展,前端將建設發展教育研發、健康預防、醫學檢測,後端將建設發展綜合康復、醫療旅遊,現已引入了四川臍血幹細胞、臺灣美兆、北京博奧、華西醫院、美國ICTWA再生等醫學企業。產業集群化落腳于分子診斷產業,可以推動技術流動、資源互補、產業合作、資訊擴散、費用節省等。 與會的嘉賓對成都國際醫學城的發展模式表達了強烈的興趣。程京院士表示,成都和重慶對於醫學發展都非常的重視,國際醫學城設計理念超前,入駐企業都非常的優秀。韓德民院長表示,成都國際醫學城以分子診斷和健康為主打項目,是非常好的選擇,也符合未來中國醫學的發展方向。解放軍301醫院生命科學院副院長王曉甯認為,成都國際醫學城的產業集群的模式非常的好,哪里能改變模式,哪里的新興產業就能發展。溫州醫學院藥學院院長李校堃也非常贊同成都國際醫學城的發展方式。

藥物基因體vs 70餘種藥物美國FDA批准貼上遺傳標籤

分子診斷產業化發展及市場前景解讀

生物谷  2011-04-13分子診斷市場的現狀及前景如何?怎樣才能更好的發展這一產業?  201148下午,由成都國際醫學城主辦,生物谷承辦,博奧生物特別支持的分子診斷產業高峰論壇(第二屆中國分子診斷技術大會分論壇)在重慶隆重召開,此次論壇主題是\"推動轉化醫學,發展產業集群,服務人類健康。與會的眾多專家圍繞上述問題展開了精彩的演講和討論,贏得了來自行業內百餘位參會者的陣陣掌聲。中國工程院院士程京,溫江區副區長、成都國際醫學城指揮部指揮長何敏,北京同仁醫院院長韓德民,解放軍301醫院生命科學院副院長王曉甯,新疆醫科大學附一院院長溫浩,溫州醫學院藥學院院長李校堃,生物谷集團董事長兼總裁張發寶以及中南大學臨床藥理研究所副所長張偉教授分別發表了精彩的演講。

分子診斷市場的發展前景與機遇 據統計,2010年,全球體外診斷市場的規模逾400億美元,分子診斷占體外診斷市場的9.6%左右。中國的分子診斷市場每年的增長速度達到20%以上。據生物谷集團董事長兼總裁張發寶博士介紹,目前,分子診斷主要應用於醫院的臨床各科診斷中,將來,分子診斷有望更廣泛的應用於腫瘤個性化治療  、昂貴藥物治療監測、藥物代謝基因組學等方面。從用藥的個體化差異出發,體重、身高、性別、遺傳、病程、環境等各種因素都會影響到藥物的作用,其中最主要的因素是遺傳因素。中南大學臨床藥理研究所副所長張偉教授介紹到,每年6.7%  的住院病人都會產生嚴重藥物不良反應,同時,沒有一種藥物對所有的人群都是安全有效的,通常情況下,全球\"重磅炸彈\"級藥物的有效性也不過40%-60%。目前,70餘種藥物經美國FDA批准貼上了遺傳標籤,用於指示不同基因型的患者在應用該藥物時對療效和毒性的指示作用。個體化用藥將會成為未來的發展趨勢,基因檢測將會發揮它獨特的優勢,指導著新藥的研發及應用。分子診斷將來還有望普遍應用于人群健康篩查與體檢、重大疾病預警與診斷、公眾分子基因檔案建立等更為廣泛的方面。隨著醫療模式的轉變,越來越多的人開始關注預防,隨著這種需求的增加,將會刺激著分子診斷市場不斷發展。

What is the competitive edge at drug R&D? Innovation or consistency?

China making big gains in drug R&D jobs state covets

Greg AndrewsApril 9, 2011  Here in a gleaming new building, Crown employees are conducting high-end early-stage research on new drugs—and doing so at what by U.S. standards are bargain-basement prices. The total annual cost for one researcher at Lilly might run $300,000 to $350,000 a year. The figure at Crown is one-third of that, said Chuan "Joe" Shih, Crown's executive vice president of integrated drug discovery. Former Lilly researcher Shih helps lead one of the many drug R&D firms in the Shanghai area. The Taiwanese-born Shih ought to know. He spent 25 years as a researcher at Eli Lilly, attaining the lofty company title of distinguished scholar. He left two years ago for the senior management post at Crown—part of a throng of fast-growing contract-research organizations in China. Crown won't divulge its full list of clients. But it includes heavyweights, including New York-based Pfizer Inc. Lilly and many other pharmaceutical firms also are outsourcing an increasing amount of drug research here, as they struggle to lower drug-development costs and get new drugs to market faster. The entire industry is under unprecedented pressure as patents expire on the current crop of blockbusters. "Many, many companies come to this part of the world because of the lower cost and the talent," said Shih, co-inventor of Lilly's Alimta, a lung cancer drug with $2.2 billion in annual sales. He said the Chinese government adds to the allure of using CROs here by providing them lucrative incentives that further reduce expenses. Faming Zhang, a former Lilly executive and Indiana University professor, founded Crown five years ago. Company officials have raked in tens of millions of dollars in venture capital and eventually hope to take the company public. They certainly have plenty of growth to tout. Crown employs 180 in Beijing and another 170 outside Shanghai, and the company plans to add another 180 outside Shanghai by the end of this year. Researchers work in laboratories to create potential new drugs and test them on mice, monkeys and other animals.

Emerging competitor  The emergence of firms like Crown is a worrisome trend for the U.S. economy, said Benjamin Shobert, managing director of Teleos, an Indianapolis consulting firm. "It could be the same sort of threat we face in manufacturing. But America believes it can afford to give away some of our high-labor-content, low-value-added manufacturing. We have to keep this kind of work," Shobert said. "We have to show that, 'Yeah, we're more expensive, but we produce much more high-quality outputs,' or we'll lose that, too." For now, U.S.-trained scientists do maintain an edge over China-trained scientists, who generally have most of the basic skills they need but are less adept at creative problem solving, Shih said. "You just have to develop a very good environment to nurture them and push them," said Shih, one of several experienced researchers who worked in the United States and now are part of Crown's management team. Lilly's CRO partners in China include WuXi AppTec and ChemExplorer. It also operates its own research-and-development center in Shanghai and is building a diabetes research center here. The company hasn't abandoned central Indiana, by any means. It still employs more than 10,300 people in the region, many in R&D. But in an interview in Shanghai with IBJ last month, Lilly CEO John Lechleiter said CROs in China have more to offer than cost savings. "The skill level and the quality and the increasing availability of high-skilled and high-quality operations in the contract-research space renders these firms globally competitive," he said. Asked whether the emergence of high-quality pharmaceutical research in China puts research at risk in the United States, Lechleiter said: "There is not one easy answer. I will say I think our research tends to migrate to where the intellectual capital sits." In recent years, he said, Lilly has had difficulty getting green cards or permanent resident visas for some of the Chinese people graduating from American universities it wants to hire. "So we need to follow the talent, and I expect there will be people recruited to the U.S. who will want to stay in the U.S. And there will be Chinese people and others who want to come back here. Our research center in Shanghai gives them a place to land." Putting R&D in China also helps position companies to sell into the huge, emerging Chinese market, said Rachel Gong, an independent health care consultant in China. But the cost savings are particularly compelling given the struggling pharmaceutical industry's need to invent new drugs quickly and the high risk of failure. In the United States, a $100 million investment might advance just one or two drugs to late-stage development, she said. In China, that money might advance 10.

中國試辦新藥開發和CRO企業海關優惠

國際服務外包保稅監管試點正式啟動

中國品質新聞網  2010-04-07 08:26:27    325,上海海關、張江集團在張江高科技園區舉行上海海關國際服務外包保稅監管試點啟動儀式,浦東海關向首批試點企業美藥典醫藥標準物質研發(上海)有限公司、上海睿智化學研究有限公司頒發保稅監管手冊,合同備案金額共計人民幣1610萬元,這標誌著上海地區國際服務外包海關保稅監管工作正式開始。浦東新區是上海市服務外包產業聚集地,對服務外包進口貨物實行保稅監管是海關促進新區現代服務業發展,支持浦東新區綜合配套改革和二次創業的重要舉措,也是海關"主動作為",將保稅監管和服務從"加工貿易"領域拓展到"服務貿易"領域,推動加工貿易轉型升級的一個有益嘗試。 新政策允許海關對管理類別為B類及以上的技術先進型服務外包企業、從事國際服務外包業務外商免費提供的設備類貨物實施保稅監管,這一新的保稅監管措施有四方面優勢,一是可以大幅簡化貨物進口手續;二是大大提高通關效率;三是減輕企業資金壓力;四是可以免除企業提交部分許可證件的要求,方便貨物進口。國際服務外包保稅監管手冊的生成,將進一步提高企業的國際競爭力,促進上海地區國際服務外包產業的發展,推動區域經濟產業結構的調整和優化升級。  "在上海市科委批准的105家技術先進型服務企業中,有42家落戶在張江,"上海張江(集團)有限公司副總經理殷宏在啟動儀式上說,"海關在張江園區率先對技術先行型服務企業推出保稅監管的嘗試,將為園區從事新藥開發和研發外包服務的生物醫藥企業、跨國研發中心的各類研發設備進出口提供便利,有效地降低其成本支出。此舉也為園區技術先進型服務企業的快速發展注入了新的活力,為我國服務外包進口貨物實行保稅監管創新改革提供探索依據,積累管理經驗,對園區實施服務外包戰略,實現企業國際化、科技化和產業化發展具有重要意義。"

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