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validation master plan中文是什么意思
发音:
- 中文翻译
- 造句
- 验证总计划
- master plan 总计划。
- master plan and detail plan 主要计划及细部计划
- a master plan of the building 建筑的总体规划
- airport master plan 机场主计画
- approved master layout plan 核准总纲发展蓝图
- asian railway master plan 亚洲铁路总计划
- capital master plan 基本建设总计划
- drainage master plan 雨水排放整体计划
- drainage master plan studies 雨水排放整体计划研究
- implementation strategy for master plan 总体规划实施战略
- industrial master plan 工业总规划; 工业总计划
- master city plan 城市总体规划
- master construction schedule plan 施工总进度计划
- master development plan 总发展计划图
- master game plan 主行动计划
- master landscape plan 园景设计总图
- master layout plan 总纲发展蓝图
- master plan for asia and the pacific 亚洲及太平洋总计划
- master plan for tourism 旅游总体规划
- master plan of holes 开孔总布置图
- master plan of operations 业务总计划
- master plan position indicator 主控平面位置显示器
- master plan,comprehensive planning 城市总体规划
- master plot plan 全厂布置图, 总平面图, 总规则
- validation of access to a segment 确认对某段访问的合法性
- validation in remote sensing 遥感的真实性检验
- Complete and perfect qualification master plan and validation master plan
完成和完善确认主计划和验证主计划。 - In case of large projects , it may be necessary to create separate validation master plans
如果项目庞大，则需要制定分开的验证主计划。 - Prior to full - scale operation , the validation master plan should be finalized . most often , this should contain three sections : strategy , protocols , and evaluation
全面运转之前，应完成鉴定总计划。通常应该包含三部分：策略、协议和评估。 - For establishing validation policy and procedures for k - company non - sterile dosage forms , a comprehensive validation master plan has been written as attached
为了建立k公司非无菌制剂的验证方针和规程，需要全面的验证主计划，如附件所示。 - All validation activities should be planned . the key elements of a validation program should be clearly defined and documented in a validation master plan ( vmp ) or equivalent documents
所有验证活动都要进行规划。验证计划的关键组成部分应该明确定义并在验证主计划（ vmp ）或类似文件中写明。
The Validation Master Plan also referenced as "VMP" is one of the key documents in the GMP (Good manufacturing practice) regulated pharmaceutical industry. Even though it is not mandatory the Food and Drug Administration inspectors will ask you for it when they inspect your facility.
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Last modified time:Sun, 10 Aug 2025 00:29:56 GMT
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