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apailles de couleur blanche avec logo d impression 白色颜色秸杆与商标D印象 [translate]
aSUPPLIED, INSTALLED & COMMISSIONED DURING LAST SEVEN(07) YEARS 在为时七(07)年期间，供应，安装&委任 [translate]
ayou haveto 您haveto [translate]
aTransportation of materials glazing 材料给上釉的运输 [translate]
aDionk Dionk [translate]
aThis page allows you to identify natural variants of Arabidopsis and closely related species using various parameters. 这页允许您使用各种各样的参量辨认Arabidopsis和紧密地相关的种类自然变形。 [translate]
aand distribution 并且发行 [translate]
a我 我的 fong 瓷器 [translate]
aused up 用完 [translate]
ashe hopes to be promoted 她希望被提升 [translate]
aIssuing Procedures 发布规程 [translate]
aco-shipment co发货 [translate]
aThe Trusted Commission 1947, The Benham Committee 1950, The Bain Commission for Sabah and Sarawak 1956, The Watson Commission for Sabah and Sarawak 1962 被信任的委员会1947年， Benham委员会1950年， Bain委员会为Sabah和Sarawak 1956年，华森委员会为Sabah和Sarawak 1962年 [translate]
aNot to Miss 不对小姐 [translate]
aPlease keep to pull in balance order that we still be short of this duct . 拉扯平衡顺序的请保留那我们仍然是这条输送管短小。 [translate]
aNeuronal 神经细胞 [translate]
asales in advance for information on applications in which exceptional reliability is required 事先销售对于信息关于例外可靠性需要的应用 [translate]
aYuyao L&F Industry Co., Ltd. Yuyao L&F产业Co.，有限公司。 [translate]
atest programme 3n 测试程序3n [translate]
aOne critical component of the submission is the highly detailed draft package insert, which is usually developed by Regulatory Affairs, Clinical Development, and Marketing using information gathered during all phases of clinical trials. The insert specifies indications for the new medicine; explains dosage and administ 提议的一个重要组分是高度详细的草稿包裹插入物，由管理事理、临床发展和行销通常开发使用在所有阶段收集的信息临床试验期间。 插入物为新的医学指定征兆; 解释剂量和管理指南; 并且提供关键声明关于安全、行动风险、机制和其他特征。 理想地，草稿包裹插入物与在发现期间建立的目标产品外形是一致的，以次要变化反射药物发展的结果。 [translate]
a• New formulation of a previously approved drug (but not a new entity or new salt) • 一种早先批准的药物，但不是 (新的个体或者新的盐的新的公式化) [translate]
aPlace of issue 签发地点 [translate]
aMr. Turner is a careless man .he often forgot something and his friends call him Mr forgetfull. one afternoon he got home but found 先生。 特纳是.he经常忘记的一个粗心大意的人某事和他的朋友称他forgetfull先生。 一个下午他得到了家庭，但发现 [translate]
aThe benefits of CSR are not homogeneous, and effective CSR initiatives are not generic. CSR的好处不是同类的，并且有效的CSR主动性不是普通的。 [translate]
aUnlike many other clinical trials, Phase IV studies are not typically randomized or placebo controlled. Instead, these trials are "open label" all subjects are given the newly approved product, and they and their caregivers know what that product is. Medical Affairs teams often conduct these studies. (See Chapter 6) 不同于许多其他临床试验，阶段IV研究没有被随机化或安慰剂没有典型地被控制。 反而，这些试验是“开放标签”给所有主题最近被批准的产品，并且他们和他们的照料者知道什么那个产品是。 医疗事理队经常进行这些研究。 (看第6章) [translate]
aClinical Development must be seen as more than a series of discrete steps or phases. We will therefore step back to look at how the entire process unfolds. The heart of clinical development is the clinical trial or study, which is a complex, carefully regulated activity. Each study is executed in compliance with a 必须看临床发展作为更多 比一系列的分离步或阶段。 因此我们将跨步回到神色在怎样整个过程展开。 临床发展的心脏是临床试验或研究，是复合体，仔细地被调控的活动。 每项研究被执行依从起一roadrnap作用对于试验每个阶段，从调查员和患者补充通过数据分析的一个详细的研究协议。 (看图5.16) [translate]
aGood morning baby , today is cold take care 早晨好婴孩，今天是冷的小心 [translate]
aSome of your students had come to our summer camp in recent years. So it’s our pleasure to recommend our Summer Camp Program. We would like to cooperate with your school for group. 你的一些学生近年来来了到我们的夏令营。 如此它是我们的乐趣推荐我们的夏令营节目。 我们希望与您的为小组的学校合作。 [translate]
aThe protocol must be approved by an institutional review board (I1 必须由一个协会评论委员会批准协议 (I1<.B) 参加与每个参与站点。 怒火由representa¬tives组成从地方社区，包括科学家，医师，道德家，和 [translate]
议定书 》 必须由一个机构审查委员会批准 （I1 <。B） 与每个参与站点隶属关系。IREs 组成的 representa¬tives 从当地社区，包括科学家、 医生、 伦理学家和
apailles de couleur blanche avec logo d impression 白色颜色秸杆与商标D印象 [translate]
aSUPPLIED, INSTALLED & COMMISSIONED DURING LAST SEVEN(07) YEARS 在为时七(07)年期间，供应，安装&委任 [translate]
ayou haveto 您haveto [translate]
aTransportation of materials glazing 材料给上釉的运输 [translate]
aDionk Dionk [translate]
aThis page allows you to identify natural variants of Arabidopsis and closely related species using various parameters. 这页允许您使用各种各样的参量辨认Arabidopsis和紧密地相关的种类自然变形。 [translate]
aand distribution 并且发行 [translate]
a我 我的 fong 瓷器 [translate]
aused up 用完 [translate]
ashe hopes to be promoted 她希望被提升 [translate]
aIssuing Procedures 发布规程 [translate]
aco-shipment co发货 [translate]
aThe Trusted Commission 1947, The Benham Committee 1950, The Bain Commission for Sabah and Sarawak 1956, The Watson Commission for Sabah and Sarawak 1962 被信任的委员会1947年， Benham委员会1950年， Bain委员会为Sabah和Sarawak 1956年，华森委员会为Sabah和Sarawak 1962年 [translate]
aNot to Miss 不对小姐 [translate]
aPlease keep to pull in balance order that we still be short of this duct . 拉扯平衡顺序的请保留那我们仍然是这条输送管短小。 [translate]
aNeuronal 神经细胞 [translate]
asales in advance for information on applications in which exceptional reliability is required 事先销售对于信息关于例外可靠性需要的应用 [translate]
aYuyao L&F Industry Co., Ltd. Yuyao L&F产业Co.，有限公司。 [translate]
atest programme 3n 测试程序3n [translate]
aOne critical component of the submission is the highly detailed draft package insert, which is usually developed by Regulatory Affairs, Clinical Development, and Marketing using information gathered during all phases of clinical trials. The insert specifies indications for the new medicine; explains dosage and administ 提议的一个重要组分是高度详细的草稿包裹插入物，由管理事理、临床发展和行销通常开发使用在所有阶段收集的信息临床试验期间。 插入物为新的医学指定征兆; 解释剂量和管理指南; 并且提供关键声明关于安全、行动风险、机制和其他特征。 理想地，草稿包裹插入物与在发现期间建立的目标产品外形是一致的，以次要变化反射药物发展的结果。 [translate]
a• New formulation of a previously approved drug (but not a new entity or new salt) • 一种早先批准的药物，但不是 (新的个体或者新的盐的新的公式化) [translate]
aPlace of issue 签发地点 [translate]
aMr. Turner is a careless man .he often forgot something and his friends call him Mr forgetfull. one afternoon he got home but found 先生。 特纳是.he经常忘记的一个粗心大意的人某事和他的朋友称他forgetfull先生。 一个下午他得到了家庭，但发现 [translate]
aThe benefits of CSR are not homogeneous, and effective CSR initiatives are not generic. CSR的好处不是同类的，并且有效的CSR主动性不是普通的。 [translate]
aUnlike many other clinical trials, Phase IV studies are not typically randomized or placebo controlled. Instead, these trials are "open label" all subjects are given the newly approved product, and they and their caregivers know what that product is. Medical Affairs teams often conduct these studies. (See Chapter 6) 不同于许多其他临床试验，阶段IV研究没有被随机化或安慰剂没有典型地被控制。 反而，这些试验是“开放标签”给所有主题最近被批准的产品，并且他们和他们的照料者知道什么那个产品是。 医疗事理队经常进行这些研究。 (看第6章) [translate]
aClinical Development must be seen as more than a series of discrete steps or phases. We will therefore step back to look at how the entire process unfolds. The heart of clinical development is the clinical trial or study, which is a complex, carefully regulated activity. Each study is executed in compliance with a 必须看临床发展作为更多 比一系列的分离步或阶段。 因此我们将跨步回到神色在怎样整个过程展开。 临床发展的心脏是临床试验或研究，是复合体，仔细地被调控的活动。 每项研究被执行依从起一roadrnap作用对于试验每个阶段，从调查员和患者补充通过数据分析的一个详细的研究协议。 (看图5.16) [translate]
aGood morning baby , today is cold take care 早晨好婴孩，今天是冷的小心 [translate]
aSome of your students had come to our summer camp in recent years. So it’s our pleasure to recommend our Summer Camp Program. We would like to cooperate with your school for group. 你的一些学生近年来来了到我们的夏令营。 如此它是我们的乐趣推荐我们的夏令营节目。 我们希望与您的为小组的学校合作。 [translate]
aThe protocol must be approved by an institutional review board (I1 必须由一个协会评论委员会批准协议 (I1<.B) 参加与每个参与站点。 怒火由representa¬tives组成从地方社区，包括科学家，医师，道德家，和 [translate]
