Effectively Supporting Clinical Sites for Continuous Audit Readiness

Discover strategies to navigate complex compliance requirements, initiate CAPAs and support clinical sites for audit readiness. With this webinar you will acquire a clear understanding of how to effectively support your clinical sites for every stage of the inspection process to ensure that regulatory expectations are met and any audit findings are managed effectively.

The expert speaker will share with the attendees how to attain good clinical practice (GCP) compliance for sponsors and clinical sites, including the assessment and improvement of quality management systems (QMS), site qualification, audit and inspection readiness. The identification and mitigation of risks such as protocol deviations, data discrepancies, data protection deficiencies and documentation gaps will also be covered.

Attendees will acquire insights into how to initiate corrective and preventive actions (CAPAs) and/or change control processes as necessary. In addition, this webinar offers attendees guidance on conducting comprehensive reviews of essential records, procedures and other internal quality documentation to ensure overall compliance with regulatory standards, study protocols and procedures.

Register for this webinar today to learn strategies that will assist in supporting clinical sites for audit readiness.

Keywords: Quality Control, CRO, Clinical Operations, Regulatory, Quality Assurance, Quality Management, QA, Quality Management System, Sites, Quality, Audit & GCP Compliance

Others Details

Life Sciences,Pharmaceutical Regulation,Pharma