A list of Standard Operating Procedures (SOPs) and supporting templates, grouped under relevant areas of research governance and clinical research. These SOPs provide clear, practical guidance on the management and day-to-day conduct of clinical research, helping you stay compliant, efficient, and confident at every stage of your study.Please refer to these pages regularly, as the most up-to-date versions will be published here. Administration Processes for managing documentation, record-keeping, and operational support to ensure efficient clinical research administration. Clinical Research Procedures for conducting clinical studies, ensuring compliance with ethical, regulatory, and scientific standards. Governance and Sponsorship Procedures for research governance, sponsorship responsibilities, and regulatory compliance to uphold integrity and accountability. Quality Assurance QA procedures for preparing and version controlling documents and performing vendor assessments. Monitoring Procedures for overseeing research studies, ensuring adherence to protocols, regulatory requirements, and data integrity. Pharmacovigilance Processes for identifying, documenting, and reporting adverse events and safety concerns to protect participants and maintain compliance. Human Resources Procedures for staff training, roles, and responsibilities to support a skilled and compliant research workforce. BioResource Access BioResource SOPs. This article was published on 2024-11-27
