In Depth Testing of Computer Systems Regulated by FDA
July 12, 2018 - Online Event ON CA
Phone: 416-915-4438/ 58
Effective and compliant computer system validation is critical to any pharmaceutical or FDA-regulated organization. FDA requires that all computer systems used to produce, manage and report on GxP (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. You must follow best practices for developing a validation program that includes planning, execution and maintenance components to ensure that these efforts will meet all regulatory agency requirements and expectations. Preparedness will improve your relationship with the agency and ensure a more cooperative and successful audit experience. Join this session with expert speaker Carolyn Troiano to learn all about preparing your system validation documentation for an FDA audit of your company’s computer systems.