DIAアカウントをお持ちの場合、サインインしてください。

サインイン

ユーザーIDをお忘れですか? or パスワードをお忘れですか?

メニュー 戻る Informed-Consent

Digital Learning Catalog

DIA Learning: eLearning Soultions
Download

Informed Consent: Comprehensive Concepts and Components eLearning Module

Informed Consent: Comprehensive Concepts and Components eLearning Module

This comprehensive module provides the key concepts of informed consent. It explains the components of a complete and appropriate consent form as specified by the International Conference on Harmonisation (ICH) and the US Food and Drug Administration (FDA), as well as guidance for the creation and appropriate wording of these components. It also includes a discussion on the benefits and concerns with electronic informed consent, and presents publications and projects that explore the use of eConsent.

Featured Topics
  • Determining When Informed Consent Is Necessary
  • Comprehension Guidelines
  • Overview of Elements of Consent
  • Writing the Introduction and Purpose Statement
  • Explaining Procedures
  • Explaining Risks and Benefits
  • Explaining Alternatives, Cost, and Compensation
  • Explaining Confidentiality and Subject Rights
  • Storage of Specimens
  • Contact Information, Consent Statements, and Signatures
  • Long Form versus Short Form, and Tips for Administering Consent
  • Changes to Informed Consent Under HIPAA

Learn more

Add Module to Cart



Related Products

Clinical Trial Management Comprehensive eLearning Bundle

This eLearning bundle includes the Clinical Trial Fundamentals eLearning Program and the Informed Consent: Comprehensive Concepts and Components module.

Learn more

Add Bundle to Cart



Clinical Trial Fundamentals eLearning Program

This eLearning program is designed to provide a practical context to help clinical research professionals learn about conducting clinical trials. Using an interactive case study with realistic scenarios designed to illustrate the learning points, the program follows the activities of a fictitious clinical investigator and her staff as they conduct a clinical trial. The program includes three modules that focus on study preparation, study initiating, and conducting a study.

Learn more

Add Program to Cart


最新情報や機会を逃さないで

DIAのメールを購読すれば、常に最新の業界情報やイベント情報を得ることができます。