Learn policies and procedures required to support activities related to computer system validation for systems subject to FDA regulations in this webinar.
Get trained on practical aspects of FDA process validation, equipment qualification, Data analysis, statistical tools for Process Quality Management, more.
Learn how computer system validation can be applied to mobile applications subject to FDA regulations, what are the best practices, trends in validation.
Learn about the best planning approach for guaranteeing foremost business edges and achieving Food and Drug Administration compliance through this webinar.
Webinar will provide an understanding of current expectations of ISO 13485 notified body auditors regarding containment or correction of nonconformity.
Learn about the FDA published final rule on Electronic Medical Device Reporting so that your company can be ready, and the requirements for submitting MDR reports electronically
Learn about requirements for defining, documenting, implementing a complaint-handling system, complaint review, investigation, corrective action, more.