EDC Inspection Readiness for Clinical Sites

Courses

Prerequisites

すべてのロール用またはロール専用のRave EDC エッセンシャル

Overview

このコースは、規制当局による実地調査の際に、質問が予想される事項等のガイダンスを、特にRave EDCの使用に焦点をあてて、治験担当医師およびCRCに提供します。査察官からの想定質問を多数レビューするほか、規制当局の観点から最も重要である「Rave EDCを使ってどのように治験を行ったか」という点についてもガイダンスを提供します。

コースの履修単位を取得するには、最後に確認試験に合格する必要があります。

グローバルエデュケーショントレーニングセッションの録音・録画は固く禁じられています。トレーニングを録音・録画しようとするとトレーニングは即座に停止され、その行為を中止するまで再開されません。

Course Type

eラーニング

Audience

Monitors, Site Personnel

Duration

~30分

Languages

English

Product

Rave EDC (Legacy)

Training Units

N/A

Course Supplements

コース概要 − 規制当局調査の準備：医療機関用

Payment Method

If paying by Purchase Order (PO), please e-mail an authorized PO to invoicing@mdsol.com. You will be invoiced for the full amount of the training class with net 30 terms in the month following training. PO must be received 5 business days prior to the start of the class to guarantee enrollment.

Existing Agreement
To schedule a public training utilizing an existing agreement, please contact your Medidata Project Manager.

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EDC Inspection Readiness for Clinical Sites

Prerequisites

Overview

Course Supplements

How To Register