{"id":48774,"date":"2022-09-26T12:01:42","date_gmt":"2022-09-26T10:01:42","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/fda-trends-for-computer-system-validation-csv-compliance-and-enforcement-virtual-seminar-researchandmarkets-com\/"},"modified":"2022-09-26T12:01:42","modified_gmt":"2022-09-26T10:01:42","slug":"fda-trends-for-computer-system-validation-csv-compliance-and-enforcement-virtual-seminar-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/fda-trends-for-computer-system-validation-csv-compliance-and-enforcement-virtual-seminar-researchandmarkets-com\/","title":{"rendered":"FDA Trends for Computer System Validation (CSV) Compliance and Enforcement (Virtual Seminar) – ResearchAndMarkets.com"},"content":{"rendered":"
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DUBLIN–(BUSINESS WIRE)–The “4-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement”<\/a> webinar has been added to ResearchAndMarkets.com’s<\/strong> offering.\n<\/p>\n

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\nUpon completion of this session, attendees will have an understanding of FDA compliance and enforcement as it relates to computer system validation.\n<\/p>\n

\nThey will understand how to develop the most robust computer system validation compliance program, focusing on the critical areas of interest to FDA. The attendees will have a good grasp of how to identify potential weaknesses and findings, as well as how to make recommendations for addressing and remediating them through risk mitigation.\n<\/p>\n

\nIn particular, we will focus on best practices for validating computer systems regulated by FDA and meeting compliance with electronic records and electronic signatures (21 CFR Part 11). We will also provide current FDA trends, including a focus on data integrity issues in the industry, which will be illustrated through industry examples.\n<\/p>\n

\nThe Seminar will cover what you need to do to prepare for an FDA audit, and also the importance and steps required to be certain you have audited all vendors of regulated systems appropriately.\n<\/p>\n

\nWhy you should attend<\/strong>\n<\/p>\n

\nEffective and compliant computer system validation is critical to any FDA-regulated organization. FDA has set forth very specific requirements for meeting compliance, and a very prescriptive set of enforcement actions to protect patient and\/or consumer safety.\n<\/p>\n

\nThis course will enable you to best anticipate and prepare for FDA scrutiny, understand your role during inspections and audits, and gain insight to the level of enforcement associated with various findings, consent decrees and warning letters. Examples from industry will be used as case studies to illustrate these.\n<\/p>\n

\nIt is vital for regulated companies to maintain a pulse on the regulatory environment in order to fortify system validation efforts, as necessary, to meet FDA expectations. It is the best practice to have a robust computer system validation, continue executing against it consistently, and documenting it thoroughly.\n<\/p>\n

\nBy maintaining a strong and consistent computer system validation program, companies can further build trust with FDA and the consumers who rely on such oversight for protection.\n<\/p>\n

\nWho Should Attend:<\/strong>\n<\/p>\n