℡_Ｇōｄ?之讨论团P5V5最佳实用队伍

冬蔷薇

淡定的蛋蛋 发表于 2012-5-20 13:24
额，LZ比较自信，容不得别人质疑他的理念，习惯就好。
综合来说，3.7夺冠的忍队，对暗杀的依赖还是比较大 ...

汗，我那坑爹忍者，一到半决赛就看不见暗杀了，基本都是靠忍者拉仇恨，用咒和魔宠把对方耗死
持久战中基本暗出来一个就结束了

芽芽

冬蔷薇 发表于 2012-5-20 12:50
在6.0那边偶尔觉得任务PK战术战略有点匮乏了
偶尔会到3.7和7.0吸收点知识
看来各各版本都有见贴就喷的人 ...

见笑了

飞鸿别恋11

我可没说过，有忍就没有技术，请认真看看贴，我拿冠军也靠的是忍

飞鸿别恋11

我可没说过，有忍就没有技术，请认真看看贴，我拿冠军也靠的是忍，带忍出暗杀的情况下比较容易打而已

℡_Ｇōｄ?Ryo

真不知道6.0是什么样子，有时间我会去看看6。0的比赛视频的

℡_Ｇōｄ?Ryo

你们这些发广告的是不是脑残？

℡_Ｇōｄ?Ryo

你们这些广告的是不是脑残？

lvae416f

?(Reporter Zhang Ran) Yesterday, the State Food and Drug Administration issued "to strengthen the relevant provisions of the supervision and management of pharmaceutical excipients (draft)" (hereinafter referred to as "draft"), to the public for comments. "Draft" to be used in the production of drugs in the pharmaceutical excipients according to the standard inspection. The pharmaceutical excipients used in the production and dispensing of pharmaceuticals, excipients and additives. The pharmaceutical excipients is an important part of drugs, can directly affect the quality and safety of drugs. "Draft" made it clear that the pharmaceutical preparations manufacturing enterprises is the responsibility of the quality of medicines, pharmaceutical preparations manufacturing enterprises must be of pharmaceutical production accessories used in strict control, and supplier audit. Medicinal materials purchased must be used in the production of drugs 0638. "Draft," stressed that the manufacturers of pharmaceutical preparations must be prescribed prescription process the production of drugs, if the change should be in accordance with the relevant provisions of the study, and to fulfill the formalities for change. "Draft" reference to the pharmaceutical excipients pharmaceutical raw materials management, and increased supervision: either the pharmaceutical excipients manufacturers to organize production in accordance with the "pharmaceutical excipients production quality management practices" to improve the production enterprise access threshold ; two excipients into different categories according to risk management, materials and production of high-risk enterprises, strict access system, and strengthen risk control; new drug with excipients and pharmaceutical preparations associated review, emphasizing the pharmaceutical manufacturers of new excipients inspection and audit responsibilities, and further tightened to further enhance the drugs are drugs with stationary sources, and technical requirements of the excipients; will enhance and improve the standard of the pharmaceutical excipients as the current focus, the quality of pharmaceutical preparations. The comments deadline is June 8.

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