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尽管药物对人类保健事业的贡献是人所周知的,而且近年来医药工业的发展速度是令人乐观的,但具有药物研究与开发功能的许多国外制药工业都发现了在继续发展中的不少问题。这些问题虽然还不足以影响目前的发展速度,但对未来的影响相当明显。1 被夸大的药品危险和过分严格的管理法规如何正确评价药物的副作用和毒性,尤其是远期毒性?是制药界与管理机构有观点分歧的地方。双方对高效、低毒、价廉等社会对药品的要求的认识是一致的,但在寻找“安全”和“发展”之间的平衡点时产生了
Although the contribution of medicines to human health is well known and the pace of development of the pharmaceutical industry has been encouraging in recent years, many foreign pharmaceutical industries that have the function of drug research and development have found that many continue to develop problem. Although these problems are not enough to affect the current pace of development, the impact on the future is quite obvious. Exaggerated drug risks and overly stringent regulatory regulations How to correctly evaluate side effects and toxicity of drugs, especially long-term toxicity? There are differences of opinion between the pharmaceutical industry and regulatory agencies. The two sides agreed on the requirements of the society for drugs with high efficiency, low toxicity and low cost, but they came up with the search for a balance between “security” and “development.”