Essential Components of a Clinical Trial Agreement | Webinar Series
Clinical trials produce valuable data and knowledge that can benefit the scientific community and the public. However, they also raise complex legal and ethical issues related to the publication and dissemination of study results. In addition, there are issues involving the confidentiality of the data and interaction with the health care provider regarding protected health information, the management of study data, and the source documents including the subject medical records and any needed data sharing for verification/reproducibility. This webinar will provide an overview of the best practices and regulatory requirements for publication and data issues (confidentiality and data management) in clinical trial contracts.
Learning Objectives:
- Understand and apply the principles and standards for sharing clinical trial data with various stakeholders.
- Identify and address the legal and ethical issues related to publication rights, authorship, peer review, data quality, data ownership, intellectual property rights, data sharing agreements, and open access policies.
- Implement the best practices and regulatory requirements for ensuring the confidentiality, security, integrity, accessibility, and preservation of study data.
Individual Registration:
Member Price: $99
Non-Member Price: $165