?grantee

grantee發(fā)音

英：[grɑ:n'ti:]　　美：[grɑ:n'ti:]

英：　　美：

grantee中文意思翻譯

n.受讓人, 受頒贈者

grantee常見例句

1 、His rareness disinclined me to grant his request.───他的粗魯使我不愿意答應他的請求。

2 、They refused to grant them long-term credit.───他們拒絕給予他們長期信貸。

3 、She finds it difficult to live on her grant.───她發(fā)現(xiàn)依靠助學金難以生活。

4 、I hesitate indeed to grant pure love.───其實我是不愿承認純潔的愛。

5 、Your rudeness disinclines me to grant your request.───你的粗魯態(tài)度使我不想答應你的要求。

6 、A gift or grant; a contribution.───一件禮物或給予物;一件貢獻物

7 、Congress may not grant titles of nobility.───國會可以不授于貴族的頭銜

8 、Work closely with Program Officer in reviewing grant proposals for appropriateness to DART strategy, budget, implementation/completion timeframes, and ability of grantee to carry out proposal.───與計劃辦公室密切配合，復查批準對災難反應援救對制定的策略、預算、執(zhí)行中/已完成任務的時間表的提案，以及受救助者個人執(zhí)行提議的能力。

9 、What kind of a grant were you thinking of?───你們考慮什么樣的獎助金?

10 、Means that the grantee is a group account.───意味著被授權者是一個組帳號。

11 、Enables the grantee to access metadata.───允許被授權者訪問元數(shù)據(jù)。

12 、Pamela Grant grew up on a ranch near Dallas.───帕梅拉?格蘭特在達拉斯附近的一個大農(nóng)場長大。

13 、Would you kindly grant me an interview?───您是否能給我一次面試的機會呢?

14 、She is grant a residence permit for one year.───她被給予一張為期一年的居住證。

15 、From time to time we invite guest bloggers from grantee organizations to tell their story.───原則是這樣：我們傾向于組建一個小的精英技術團隊。1. 你是天才程序員, 而且以此為樂。

16 、Working out with Tess and Grant.───與黛絲和格蘭特一起鍛練身體吧！

17 、The contract itself provided notice of the risks, and the grantee still contracted.───合同本身規(guī)定了風險，受讓人仍然簽約。

18 、Money,property,a deed,or a bond put into the custody of a third party for delivery to a grantee only after the fulfillment of the conditions specified.───契約，合同指錢、權利、契據(jù)或契約等暫交第三者保管，待某種條件實現(xiàn)后再交付受讓人或權利人。

19 、He can grant a wish or make a dream come true.───他聽到你的祈求,使你夢想成真。

20 、Perfect costing management system was the institutional grantee of implementing the above circles.───建立完善的成本核算管理體系是以上環(huán)節(jié)實現(xiàn)的制度保證。

21 、Enables the grantee to impersonate the user.───允許被授權者模擬該用戶。

22 、The borrower is referred to as the grantee.───借款人被稱為動產(chǎn)抵押的讓與人。

23 、A passivity controller is introduced to dissipate excess energy and thereby grantee the system's stability.───在從端設計了一個無源控制器用來吸收多余能量，以保證從端無源性，從而保證加入預測器后系統(tǒng)穩(wěn)定。

24 、They refused to grant us long-term credit.───他們拒絕給予我們長期信貸。

25 、He is young, I grant, but he is wise.───他年輕，沒有錯，但他聰明。

26 、He makes a grant of land to his son.───他將土地受讓給他的兒子。

27 、Grantee The user number of the user ID receiving the permission.───grantee接收權限的用戶ID的用戶號。

28 、He has been awarded a research grant.───他得到一筆研究經(jīng)費。

29 、The DEA should grant Dr Craker his licence.───dea批準克雷克的申請乃理所當然。

30 、To grant them a peaceful and abundant year.───他們年年有余,國泰民安。

31 、Medieval system, where land was grant by a king to his aristocracy, and by the aristocrat to the peasant, on condition that each pay a service( or feudal duty) to his superior.───一種中世紀的制度：國王將土地轉讓給貴族，貴族再轉讓給農(nóng)民。條件是每個人必須向他上級服役或交稅。

32 、Are you ready to grant that I was right?───你是否愿意承認我是對的?

33 、Yet grant some small acknowledgement of ours.───但是請給我們一點點應有的承認。

34 、Enables the grantee to take ownership of the securable on which it is granted.───允許被授權者獲取所授予的安全對象的所有權。

35 、Will you grant this technical license to us ?───你們愿意向我方轉讓這項技術許可證嗎?

36 、Josie: Grant, your costume reminds me of something.───喬西：格蘭特，你的獅子裝讓我想到一件事。

37 、You can get a grant to improve your house.───你可以得到一筆撥款來修繕住房。

38 、Money, property, a deed, or a bond put into the custody of a third party for delivery to a grantee only after the fulfillment of the conditions specified.───契約，合同指錢、權利、契據(jù)或契約等暫交第三者保管，待某種條件實現(xiàn)后再交付受讓人或權利人

39 、So Pilate decided to grant their demand.───彼拉多這才照他們所求的定案。

40 、They asked Japan to grant them increased loans.───他們要求日本給他們更多貸款。

41 、If except asks grant instruction.───如若不是請賜教。

42 、He grant his neighbour a licence to use his field.───他許可他的鄰居使用他的一塊地。

43 、Grant and Lee are bracketed in history.───在歷史上格蘭特和李兩人的名字總是被一起提及的。

44 、A refusal to grant the truth of a statement or allegation; a contradiction.───否認拒絕承認某陳述或主張的真實性; 反對

45 、May the God of all grace grant this.───但愿賜全恩的神給我們這個。

46 、They gave her a grant to study abroad for one year.───他們給了她一份助學金,供她出國學習一年。

47 、He importuned me to grant his request.───他糾纏著要我答應他的請求。

48 、To grant full citizenship to(one of foreign birth).───使入國籍獲得完全的公民權（外國出生的）

49 、To grant a license to or for; authorize.───準許發(fā)放許可證；授權

50 、N No, the grantee has not been granted this permission by the grantor.───N否,授予者沒有授予被授予者該權限。

51 、G The grantee has been given this permission and can grant the same permission to another user (with grant options).───G被授予者已被授予該權限并能將同樣的權限授予其他用戶(授予權限選項)。

52 、Database username that has granted permissions on this TABLE_NAME to the listed GRANTEE.───已向列出的GRANTEE授予對此TABLE_NAME的權限的數(shù)據(jù)庫用戶名。

53 、Sorry, I have no right to grant you the money.───對不起，我沒有權力撥錢給你。

54 、For future transaction we are pleased to grant you credit facilities, and shall submit a quarterly statement.───為了將來處理方便起見，我們確認貴公司信用，并樂于給你方提供按季結算。

55 、She is grant a non- resident visa.───她被給予非本地居民簽證。

56 、Hugh Grant is a famous British actor.───休葛蘭是很有名的英國演員。

57 、The official document of such a grant.───土地專有證賦予公共土地專有權的正式文件

58 、The setbacks of grantee might incur during the process of technology transfer.3.───2.技術移轉過程中，被授權人遭遇的各項限制問題。

59 、In case that the grantee does not use the grant in the agreed way or violates the agreement in any other way, the Foundation has the right to cancel the agreement.───受助人未按協(xié)議約定使用資助或者有其他違反協(xié)議情形的，本基金會有權解除資助協(xié)議。

60 、The grantee shall demolish and remove in time such technological equipment as required by the grant contract.───出讓合同中規(guī)定必須拆除的技術設備,受讓人應按時拆除。

61 、Steven Watt, Lenny Pidgeley, Anthony Grant.───史蒂夫-瓦特、萊尼-皮吉利、安東尼-格蘭特。

62 、Enables the grantee to impersonate the login.───允許被授權者模擬該登錄名。

63 、Heaven grant us patience with a man in love!───天??！請賜予我們以容忍戀愛中的男人的耐心吧。

64 、Can you grant me any commission?───史: 能給傭金嗎?

65 、There shall be no peace until you grant them.───你一天不答應，就一天得不到太平。

66 、He is grant a temporary injunction.───他被給予臨時禁令。

67 、He refused to grant them long-term credits.───他拒絕給他們長期信貸。

68 、If he pays a guinea to that society, the will expect them to grant him considerable privileges; he's throwing a sprat to catch a whale.───如果他捐一畿尼給這個團體，他就指望人家給他大量的特權，他是要求一本萬利的。

69 、You can get a grant to repair your house.───你可以得到一筆修房補助金。

70 、How do I get a Monash Abroad Grant?───怎樣申請蒙納士海外留學助學金?

71 、Could you grant me a premium rebate?───你能給我保險費折扣嗎?

72 、He may get a grant to study abroad next year.───他明年也許會獲得留學獎學金。

73 、Before we can give the grant we must have an estimate of the total cost involve.───在我們發(fā)補助金前，我們必須對總數(shù)有個估算。

74 、Grant me peaceful and undisturbed sleep.───恩賜我平安而不受侵擾的睡眠。

75 、How do I get a grant from the government?───怎樣得到政府的資助呢?

76 、Grant, but It's destroying one 's private life.───就算是這樣吧，但是這也會破壞人們的私生活。

77 、A supplementary grant may be awarded at the discretion of the committee.───委員會可能酌情追加一筆補助金。

78 、The pursuer requests the court to grant him remedy.───原告要求法院給予救濟。

79 、Do you wish to grant the requested access?───您想要授予所請求的訪問權限嗎?

80 、If you grant my request, you will earn my thanks.───如果你答應我的要求, 就會得到我的感謝。

ICH-GCP 6.1 Quality Assurance（1）

Part 1: Introduction

Part 2: QA and Monitoring Role

Quality Assurance (QA) in clinical trials consists of planned, systematic activities that are conducted to ensure that a trial is performed―and that trial data are generated, documented, and reported―in compliance with the protocol, Good Clinical Practice (GCP) guidelines, and all other applicable regulatory requirement(s).

臨床試驗中的 質量保證（QA）包括計劃的、系統(tǒng)的活動 ， 這些活動旨在確保試驗按照方案、良好臨床實踐（GCP）指南和所有其他適用的監(jiān)管要求進行，并生成、記錄和報告試驗數(shù)據(jù) 。

Research that is not conducted according to high standards of quality yields invalid data. It is also unethical because it may put research participants at risk. (Protection of the safety, rights, and well-being of research participants is discussed in the Introduction, Institutional Review Boards, Informed Consent, and Participant Safety and Adverse Events modules.)

沒有按照高質量標準進行的研究會產(chǎn)生無效數(shù)據(jù) 。這也是 不道德的 ，因為它可能使研究參與者處于危險之中。（引言、機構審查委員會、知情同意書以及參與者安全和不良事件模塊中討論了研究參與者的安全、權利和福利保護）

Audits conducted by the U.S. Food and Drug Administration (FDA) find that several problems commonly occur in research studies.

由美國食品和藥物管理局(FDA)進行的審計發(fā)現(xiàn)，在研究中常見的幾個問題。

Quality data are critical to ensure that the results of studies are interpreted correctly. Sloppy or incorrect data can lead to misleading conclusions. Careful attention to standards of quality also ensures that studies are completed in a timely fashion. Timely completion of high quality studies bridges the gap between research and practice by bringing effective new treatments to clients more quickly.

質量數(shù)據(jù)對于確保正確解釋研究結果至關重要。 草率或不正確的數(shù)據(jù)可能導致誤導性結論。對質量標準的認真關注也確保了及時完成研究。 及時完成高質量的研究，通過更快地為客戶提供有效的新療法，彌合研究與實踐之間的差距。

All members of the protocol team are responsible for QA.

協(xié)議團隊的所有成員 都負責QA。

While it is common for QA and monitoring-related duties and functions to be transferred to a CRO, the sponsor has ultimate responsibility for implementing and maintaining QA systems. (ICH GCP 5.1.1) This responsibility includes oversight of all QA systems as well as any trial-related functions performed or managed by other parties (i.e. the CRO, or a subcontractor to the CRO) on behalf of the Sponsor (ICH GCP 5.2.2)

雖然將QA和監(jiān)控相關職責和職能移交給CRO是常見的，但發(fā)起人對實施和維護QA系統(tǒng)負有最終責任。 （ICH GCP 5.1.1）該責任包括監(jiān)督所有 QA系統(tǒng)以及由其他方 （即CRO或CRO的分包商）代表發(fā)起人執(zhí)行或管理的任何試驗相關功能（ICH GCP 5.2.2）

Investigators and every member of the protocol team are expected to perform his or her duties diligently and thoroughly, thus ensuring that the trial is conducted according to the highest possible standards of quality.

研究人員和方案小組的每一位成員都應勤勉、徹底地履行其職責，從而確保試驗按照盡可能高的質量標準進行。

Click to view Clinical Trial Network（CTN）  related content

點擊查看臨床試用網(wǎng)絡（CTN）相關內容

The sponsor is responsible for ensuring the trial’s integrity and for developing a risk-based monitoring plan. As the sponsor of all studies conducted by the network, NIDA CTN has transferred the regulatory responsibility of all monitoring to the Clinical Coordinating Center (CCC).

申辦方 有責任確保試驗的完整性， 并制定基于風險的監(jiān)測計劃 。作為該網(wǎng)絡開展的所有研究的發(fā)起者，NIDA CTN已將所有監(jiān)測的監(jiān)管責任移交給臨床協(xié)調中心(CCC)。

The CCC develops systematic, prioritized, and risk-based (ICH GCP E6(R2) 5.18.3) monitoring plans to be utilized for each CTN study. This plan is customized for each trial and describes the strategy, methods, responsibilities, and requirements for monitoring the trial (ICH GCP E6(R2) 1.64). Additionally, the plan provides operational guidelines to ensure the quality and integrity of data collected in accordance with CTN protocols. This document also ensures consistency in the conduct of CTN studies across multiple sites and protocols. This monitoring plan:

CCC為每項CTN研究制定系統(tǒng)的、優(yōu)先的和基于風險的(ICH GCP E6(R2) 5.18.3)監(jiān)測計劃。本計劃為每個試驗定制，并描述了 監(jiān)測試驗的策略、方法、職責和要求 (ICH GCP E6(R2) 1.64)。此外，該計劃還提供了操作指南，以確保根據(jù)CTN協(xié)議收集的數(shù)據(jù)的質量和完整性。本文件還確保了跨多個站點和協(xié)議進行CTN研究的一致性。這個監(jiān)測計劃:

Ⅰ、Emphasizes the monitoring of critical data and processes.

Ⅱ、Ensures the quality and integrity of CTN clinical studies.

Ⅲ、Ensures the protection of human participants.

Ⅳ、Advances collaboration between treatment and research staff at CTN sites.

1、強調對 關鍵數(shù)據(jù) 和 過程 的監(jiān)控。

2、確保 CTN臨床研究的質量 和 完整性 。

3、確保 對人類參與者的保護 。

4、促進 CTN現(xiàn)場治療 和 研究人員之間的合作 。

The Lead Investigator (LI) is a CTN-specific role for the investigator that has overall responsibility for the entire study. The LI convenes a Protocol Team that assists with all aspects of the development and operation of the study. In other studies outside of the CTN, this role may be considered the Principal Investigator.

首席研究者（LI）是CTN特定的研究者角色，對整個研究負全面責任 。LI 召集了一個方案小組，協(xié)助研究開發(fā)和運作的各個方面 。在CTN以外的其他研究中，該角色可能被視為主要研究者。

The Project Director (or Protocol Coordinator) is the LI’s “right hand.” He or she is responsible for coordinating and carrying out day–to–day study operations. The Project Director is a member of the Protocol Team and is the primary contact for questions about the overall study. Other roles and responsibilities represented on the Protocol Team usually include, but may not be limited to, the following:

項目總監(jiān)(或協(xié)議協(xié)調員) 是 LI 的“得力助手”，他或她 負責協(xié)調和進行日常學習活動 。項目總監(jiān)是協(xié)議小組的成員， 是整個研究問題的主要聯(lián)系人 。協(xié)議團隊中代表的其他角色和職責通常包括但不限于以下內容：

Ⅰ、Data Management

Ⅱ、Quality Assurance

Ⅲ、Training

Ⅳ、Regulatory Affairs

1、數(shù)據(jù)管理

2、質量保證

3、培訓

4、監(jiān)管事務

The Node PI (or grantee) is another CTN-specific role that is responsible to NIDA for study performance at his or her Node. He or she works with Node staff, the Site Principal Investigator(s), and the Lead Investigator to implement the study at that Node. The Node PI is responsible for ensuring that the study runs smoothly at his or her Node and for taking appropriate action when necessary to assist the Site PI(s) and the Lead Investigator. Other responsibilities of the Node PI include:

節(jié)點PI（或受讓人）是另一個CTN特定角 色，負責NIDA在其節(jié)點的研究表現(xiàn)。 他或她與節(jié)點工作人員、現(xiàn)場首席研究員和首席研究員合作，在該節(jié)點實施研究 。節(jié)點PI負責確保研究在其節(jié)點順利進行， 并在必要時采取適當措施協(xié)助現(xiàn)場PI和首席研究員 。節(jié)點PI的其他職責包括：

Ⅰ、Appointing the Site PI and Study Coordinator.

Ⅱ、Managing the Node budget and staff.

Ⅲ、Appointing a monitor to conduct Quality Assurance visits at research sites within the Node.

Ⅳ、Ensuring that study staff receives appropriate training to conduct the study.

Ⅴ、Ensuring that the study receives all necessary IRB approvals and follows all applicable regulations. Knowing the policies of his or her institution/university and ensuring compliance at the Node with these policies.

1、 任命現(xiàn)場PI 和 研究協(xié)調員 。

2、 管理節(jié)點預算和人員 。

3、指定一名監(jiān)督員 對節(jié)點內的研究地點進行質量保證訪問 。

4、確保研究人員接受 適當?shù)呐嘤?進行研究。

5、確保本研究獲得 所有必要的IRB批準 并遵守所有適用的法規(guī)。了解他或她的機構/大學的政策，并確保節(jié)點遵守這些政策。

The monitoring plan sets out monitoring strategies, the monitoring responsibilities of all parties involved, the various monitoring methods to be used, and the rationale for their use. It also describes monitoring procedures, types of visits, what is involved in the conduct of those visits, and the quantity or percentage of each type of document to be monitored. These procedures can be further defined on a protocol basis depending on the purpose, design, size, complexity, and primary outcome measures of the trial (ICH GCP E6(R2) 5.18.3).

監(jiān)測計劃規(guī)定了監(jiān)測戰(zhàn)略、所有相關方的監(jiān)測責任、將使用的各種監(jiān)測方法以及使用這些方法的理由 。它還描述了 監(jiān)控程序 、 訪問類型 、 訪問過程中涉及的內容 ，以及 需要監(jiān)控的各類文件的數(shù)量或百分比 。這些程序可根據(jù)試驗的目的、設計、規(guī)模、復雜度和主要結果指標在方案基礎上進一步定義（ICH GCP E6(R2) 5.18.3).

According to GCP guidelines, “the Sponsor may choose on-site monitoring, a combination of on-site and centralized (remote) monitoring, or, where justified, centralized monitoring alone…Centralized monitoring processes provide additional monitoring capabilities that can complement or reduce the extent and/or frequency of on-site monitoring and help distinguish between reliable data and potentially unreliable data without the need for total source data verification” (ICH GCP 5.18.3). The rationale for the chosen monitoring strategy is documented in the monitoring plan.

根據(jù)GCP指南，“ 主辦方可以選擇現(xiàn)場監(jiān)測，現(xiàn)場監(jiān)測和集中(遠程)監(jiān)測相結合 ，或者，在合理的情況下， 集中監(jiān)測過程提供額外的監(jiān)測能力 ， 可補充或減少現(xiàn)場監(jiān)測的范圍和/或頻率 ，并有助于區(qū)分可靠數(shù)據(jù)和可能不可靠的數(shù)據(jù)，而無需核實全部來源數(shù)據(jù)”(ICH GCP 5.18.3)。所選擇的監(jiān)控策略的基本原理已記錄在監(jiān)控計劃中。

In general, on-site monitoring is required and remote monitoring may occur at any given research site before a trial begins, while it is in progress, and after it concludes or is terminated. In many instances, study monitors may visit each site after the first one to two participants are enrolled and then schedule subsequent visits based on multivariate criteria, such as the rate of enrollment, volume of data to review, site performance, and other considerations.

一般來說，需要進行現(xiàn)場監(jiān)測， 在試驗開始前、進行中、結束或終止后，可以在任何給定的研究地點進行遠程監(jiān)測 。在許多情況下，研究監(jiān)測人員可能會在 前一到兩名參與者登記后訪問每個位點，然后根據(jù)多變量標準安排后續(xù)訪問 ，如 登記率 、 回顧數(shù)據(jù)量 、 位點表現(xiàn) 和 其他考慮 。

Study monitors conduct site visits according to the procedures describes in the monitoring plan and in accordance with Good Clinical Practice (GCP) guidelines.

研究監(jiān)測人員根據(jù) 監(jiān)測計劃 中描述的程序并按照良好臨床實踐(GCP)指南進行現(xiàn)場訪問。

The Good Clinical Practice guidelines state that the sponsor is responsible for selecting monitors and for ensuring that the following criteria are met (see ICH GCP 5.18.2).

《良好臨床實踐指南》規(guī)定， 申辦方負責選擇監(jiān)護儀 ，并確保符合以下標準（見ICH GCP 5.18.2）。

Ⅰ、Monitors are appropriately trained and have the scientific or clinical knowledge needed to monitor the trial adequately. Monitors qualifications should be documented.

Ⅱ、Monitors are thoroughly familiar with the investigational product(s), protocol, written informed consent form, and any other written information about the trial to be provided to study participants, the Sponsor’s SOPs, GCP, and the applicable regulatory requirement(s).

1、監(jiān)護人受過適當?shù)?培訓 ，具備充分監(jiān)護試驗所需的科學或臨床知識。監(jiān)控人員的資格應該記錄在案。

2、監(jiān)護者完全熟悉 試驗藥物 、 方案 、 書面知情同意書 以及向 研究參與者提供的有關試驗的任何其他書面信息 、 申辦方的SOP 、 GCP 和 適用的監(jiān)管要求 。

QA/study monitors perform the following study activities:

QA/研究監(jiān)督員執(zhí)行以下研究活動：

Ⅰ、Conduct initiation, interim, and closeout visits.

Ⅱ、Conduct centralized monitoring, as applicable.

Ⅲ、Provide training on protocol-specific issues and Good Clinical Practice, when needed or appropriate.

Ⅳ、Follow-up on issues identified during earlier monitoring visits.

Ⅴ、File reports with the sponsor and other applicable parties, as required.

1、開展 啟動 、 臨時 和 收尾訪問 。

2、進行 集中監(jiān)控 （如適用）。

3、在需要或適當?shù)臅r候，提供關于 方案特定問題 和 良好臨床實踐的培訓 。

4、跟進 早期監(jiān)測 訪問中發(fā)現(xiàn)的問題。

5、根據(jù)需要向發(fā)起人和其他適用方提交報告。

Monitoring responsibilities are described in detail in ICH GCP 5.18.4. Click here for a summary.

ICH GCP 5.18.4中詳細描述了監(jiān)控職責。點擊這里查看摘要。

Oracle中查看用戶具有哪些權限及其相關視

查詢某個用戶具有的角色：

select grantee,granted_role from dba_role_privs where grantee='WJW';

查詢某個用戶具有的系統(tǒng)權限：

select grantee,privilege from dba_sys_privs where grantee='WJW';

查詢某個角色中具有什么系統(tǒng)權限：

select privilege from role_sys_privs where role='RESOURCE';

查詢某個角色中包含有什么角色

select granted_role from role_role_privs where role='SYSDBA';

如果想讓某個用戶擁有查看數(shù)據(jù)庫數(shù)據(jù)字典的權限，但沒有系統(tǒng)權限和針對用戶數(shù)據(jù)的權限，則可以(通常對新數(shù)據(jù)庫管理員有用)

grant create session,select_catalog_role to wjw;

管理用戶、角色和權限的DBA視圖：

DBA_USERS 提供用戶的信息

DBA_ROLES 顯示數(shù)據(jù)庫中所有角色

DBA_COL_PRIVS 顯示列級對象授權

DBA_ROLE_PRIVS 顯示用戶及其角色

DBA_SYS_PRIVS 顯示被授予系統(tǒng)權限的用戶

DBA_TAB_PRIVS 顯示用戶及他們在表上的權限

ROLE_ROLE_PRIVS 顯示授予角色的角色

ROLE_SYS_PRIVS 顯示授予角色的系統(tǒng)權限

ROLE_TAB_PRIVS 顯示授予角色的表權限

SESSION_PRIVS 顯示允許用戶使用的權限

SESSION_ROLES 顯示當前允許用戶使用的角色