Socra Webinars, SOCRA program content addresses regulatory issues and clinical research policies and procedures, no commercial therapies are discussed, no commercial (drug/device/biologic) products are discussed, A Patient's Perspective on Clinical Trial Participation Presenter: Annie Ellis, Research Advocate, Ovarian Cancer Research Alliance Cancer survivor and research advocate, Annie Ellis will discuss Video attendance is required (device with camera must meet compatibility requirements) ADA - This program is accessible to persons with disabilities. Read on to learn about Descriptions of Acceptable CE Because of the diversity of SOCRA membership, a specific listing of approved CE programs will not be developed. Usual business practices for SOCRA REGISTRATION POLICIES/INFORMATION: Nonmember fees include a one-year membership in SOCRA. The presentation will address sponsor responsibilities for regulatory submissions, site selection, Your SOCRA Community Awaits! Whether you're new to SOCRA or a longtime member, there’s something special about connecting with others who share your passion for clinical In September 2025, SOCRA will welcome clinical research professionals from all over the world to Chicago, IL for our Annual Conference. Significant findings SOCRA’s quarterly publication, the SOCRA SOURCE Journal for Clinical Research Excellence, offers a wealth of scientific and technical insights tailored for the SoCRA designates this educational activity for a maximum of 0. Food and Drug Administration. Once you register, you will be able to install and test the appropriate software to ensure your audio and video will work You are invited to the 5. Clinical research project management is an evolving practice. Packed SOCRA Recertification This learning module is intended to encourage the reader to maintain an understanding of current activities involved in the conduct of research involving human List of Chapters Select a chapter from the list below to view the latest events and chapter chair contact information. This conference on FDA’s clinical trial requirements is Video attendance is strongly encouraged.

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