This interactive, live, in-person program will be facilitated by clinical research professionals with industry and academic experience. The purpose of this program is to assist clinical research professionals in improving their understanding of the clinical research site responsibilities and apply skills and strategies to execute these responsibilities. This program is designed to address all the functions of the research site related to the Good Clinical Practices as delineated by the U.S. Code of Federal Regulations and the guidelines supported by the International Council on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH Guidelines). Recommended attendees include Site Coordinators, Research Associates, and Study Nurses.
SOCRA designates this educational activity for a maximum of 11.75 Continuing Education Credits for SOCRA CE and Nurse CNE. SOCRA designates this live activity for a maximum of 11.75 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
CME for Physicians: The Society of Clinical Research Associates is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
CNE for Nurses: Society of Clinical Research Associates is accredited as a provider of continuing nursing education by the American Nurses Credentialing Center's Commission on Accreditation.
TransCelerate BioPharma: “This ICH E6 GCP Investigator Site Training meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors.”
SOCRA Course Series: 600