FDA Clinical Trial Requirements Regulations, Compliance and GCP LIVE Conference- Nov.17-18 Includes Multiple Live Events. The next is on 11/17/2026 at 8:30 AM (EST) Already registered? Log in now. Overview Speaker(s) Contents (4) This LIVE symposium is a distinct opportunity for Sponsor-Investigators and key research staff to receive targeted training directly from FDA, NIH, and research industry representatives. It will provide insight into the unique dual-role of sponsor-investigators with in-depth coverage of the applicable FDA regulations, guidelines, and best practices. Attendees will take away tools for designing and managing quality research studies that will produce accurate and complete data submissions. The two (2) full-day schedule allows for less disruption to clinical practice and continuing education credits (CME/CNE/SOCRA CE) apply. Please contact us with any questions or concerns at education@socra.org. Please book your Hotel Room here: SOCRA FDA LIVE WORKSHOP ROOM RATE Dates: Tuesday November 17th and Wednesday November 18th, 2026. Time: 8:30 am EST to 4:00 pm EST *All times in Eastern Standard Time Zone  Registration: Standard Rate - Member Fee - $600 Standard Rate - Non-Member Fee *- $675 Continuing Education Credit: SOCRA designates this educational activity for a maximum of 11.75 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live […]

Clinical Research Professional Certification Preparation and GCP Virtual Review Course - December 2&3, 2026  Includes Multiple Live Events. The next is on 12/02/2026 at 12:00 PM (EST) Already registered? Log in now. Overview Speaker(s) Contents (4) Goal: The purpose of this workshop is to assist the participant in preparing for the CCRP certification examination. This course will review the concepts identified in the CCRP Certification Examination Content Outline, as well as the Standards of Practice including the ICH Guidelines and FDA Regulations that govern clinical research practice. Member Rate: $295.00 Non-Member Rate: $370.00 Objective: The goal will be accomplished through lecture, discussion and practical application facilitated by certified clinical research professionals with combined clinical research experience of more than 20 years. Information will be presented and discussed regarding the conduct of clinical trials; regulatory guidelines regarding IRB oversight and human research protections; ethical issues in clinical research; and workshops will stress the ability to follow directions and practices related to abstracting information and completing case report forms and other records. Please contact us with any questions or concerns at education@socra.org. Learning Objectives: Upon completion of the workshop, the attendee should be able to: Discuss the basic requirements necessary to meet the demands of a CRP in clinical […]