{"id":48448,"date":"2022-09-15T18:01:50","date_gmt":"2022-09-15T16:01:50","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/death-by-capa-corrective-and-preventive-action-seminar-researchandmarkets-com\/"},"modified":"2022-09-15T18:01:50","modified_gmt":"2022-09-15T16:01:50","slug":"death-by-capa-corrective-and-preventive-action-seminar-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/death-by-capa-corrective-and-preventive-action-seminar-researchandmarkets-com\/","title":{"rendered":"Death by CAPA (Corrective and Preventive Action) Seminar – ResearchAndMarkets.com"},"content":{"rendered":"
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DUBLIN–(BUSINESS WIRE)–The “4-Hour Virtual Seminar – Death by CAPA – Does your CAPA Program need a CAPA?”<\/a> webinar has been added to ResearchAndMarkets.com’s<\/strong> offering.\n<\/p>\n

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\nThis 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this seminar is for you.\n<\/p>\n

\nWe’ll discuss regulatory expectations, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls. We’ll discuss best practices so you can start off on the right foot and always be prepared for an inspection.\n<\/p>\n

\nThis virtual seminar provides detailed lectures on all elements of a CAPA program and how they connect to other parts of your Quality Management System. You will learn how to create a CAPA program that results in improved product quality, reduction in compliance issues, and ultimately leads to improved business success.\n<\/p>\n

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

\nCorrective and Preventive Action (CAPA) is the cornerstone of a strong Quality Management System. And yet, many medical device manufacturers struggle to establish and maintain an effective CAPA process. An ineffective CAPA process leads to disastrous consequences like complaints, recalls, 483s, and warning letters. Additionally, an inefficient CAPA system leads to wasted time and resources.\n<\/p>\n

\nCAPA is so important that it is always emphasized in FDA inspections. It is consistently one of the top reasons for 483 and Warning Letter observations. It is critical that your company establishes a compliant, effective process. This seminar will also provide tools and checklists to ensure your program is inspection ready.\n<\/p>\n

\nLearning Objectives<\/strong>\n<\/p>\n