gpo医学上是什么意思?
创始人
2025-02-01 03:11:25

gpo医学上是什么意思?

GPO是20世纪初期美国的一个药品集中采购组织。

20世纪初期,美国药品集中采购组织(Group purchasing organizations,简称GPO或者GPOs)出现,通过市场竞争将医院的需求通过GPO这样的采购中介进行集中采购。

GPO的出现为医疗机构的成本节约,减少美国医疗费用上涨的压力起到了一定的作用。

从20世纪50年代末至20世纪90年代初,美国GPO数量不断增长;采购商品也从初期购买大量的一次性用品(如注射器、导管和药品)逐渐加入了化妆品、医疗器械、手术耗材、办公用品、膳食等。服务对象也不断扩大,覆盖医疗机构,诊所,个人诊所,疗养院等。

去美国带药品有规定吗

法律分析:美国食品和药品管理局(FDA)对携带药品入境有严格规定,即使某些药物具有其他国家的医生处方,在其他国家是合法的,只要其未经FDA批准就不能入境。美海关建议入境者仅携带旅途适量必需的药物。如需携带的药物中含有潜在的成瘾性或麻醉剂成分,请务必向海关官员申报携带的所有药物。中国公民入境美国时,请一定避免携带含有麻黄碱、士的宁、吗啡、动物或动物器官等成分的中药或中成药。

法律依据:美国《Unapproved Drugs》

Preserving Patient Access to Medically Necessary Drugs

The agency balances its goal to eliminate unapproved prescription drugs from the market with patient access to medically necessary drugs. FDA carefully considers the possible effects on patient access, including whether any action would likely lead to a disruption in the drug supply, before initiating an action against an unapproved drug.

The agency permits some unapproved drugs to be marketed if they are relied on by health care professionals to treat serious medical conditions when there is no FDA-approved drug to treat the condition or there is insufficient supply of FDA-approved drugs.

FDA Approval is Required by Law

Federal law requires all new drugs in the U.S. be shown to be safe and effective for their intended use prior to marketing. However, some drugs are available in the U.S. even though they have never received the required FDA approval. Many health care professionals and patients are unaware that some of the drugs prescribed are not FDA approved.

FDA permits some unapproved prescription drugs to be marketed if:

the drug is subject to an open drug efficacy study implementation (DESI) program proceeding,

health care professionals rely on the drug to treat serious medical conditions when there is no FDA-approved drug to treat the condition,

there is insufficient supply of an FDA-approved drug.

The law allows some unapproved prescription drugs to be lawfully marketed if they meet the criteria of generally recognized as safe and effective (GRASE) or grandfathered. However, the agency is not aware of any human prescription drug that is lawfully marketed as grandfathered.

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