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1·CGMP documentation was discarded without being assessed by your quality unit.

CGMP文件记录没有经过质量部门评估就被丢弃了。

2·A very similar section on equipment cleaning (211.67) was included in the 1978 CGMP regulations.

在1978 CGMP法规中也包含了非常相似的有关设备清洗的章节(211.67)。

3·AIM: To study the effect of cGMP-dependent protein kinase (PKG) on the pathogenesis of burn shock.

目的：探讨蛋白激酶g (PKG)在烧伤休克发病机制中的作用。

4·You will also hear latest updates on various GMP and cGMP from internationally recognised regulatory experts.

您可以听到来自国际认可的法规专家带来的各国GMP的最新更新和消息。

5·In general, the hardware of a computer system is considered to be equipment within the meaning of the CGMP regulations.

通常，计算机系统的硬件被认为是符合CGMP规范的内涵的设备。

6·No. Neither the CGMP regulations nor FDA policy specifies a minimum number of batches to validate a manufacturing process.

不需要，不论cGMP法规还是FDA的政策都没有指定进行工艺验证的最少批次。

7·Therefore, the inhibition effect of Longyachongmu on specific immunity might be related to cAMP and cGMP contents in Lymphocyte.

由此推测，龙牙葱木总甙对特异性免疫功能的抑制作用可能与淋巴细胞内环核苷酸含量变化有关。

8·To ensure full compliance with the CGMP regulations, themanufacturer also should maintain adequate documentation of the correctiveaction.

为保证全面符合CGMP沙堆，生产商还应维护充分的纠正措施的文件记录。

9·In the proposed rule, FDA requested comments on current good manufacturing practice (CGMP) requirements applicable to combination products.

在法规提案中，FDA征求关于现行结合产品生产管理规范(CGMP)要求的意见。

10·Indicate whether individuals responsible for data integrity lapses remain able to influence CGMP-related or drug application data at your firm.

说明是否对数据完整性问题承担责任的个人仍有能力对你公司对CGMP相关或药物应用数据产生影响。