Advanced Certificate in Regulatory Submissions Process
-- ViewingNowThe Advanced Certificate in Regulatory Submissions Process is a comprehensive course designed to meet the growing industry demand for experts in regulatory affairs. This certificate program emphasizes the importance of regulatory submissions in bringing life-changing therapies and medical devices to market.
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Here are the essential units for an Advanced Certificate in Regulatory Submissions Process:
• Regulatory Affairs Fundamentals: An overview of regulatory affairs and its role in the product development lifecycle.
• Regulatory Submissions Process: Detailed review of the regulatory submissions process, including the preparation, submission, and maintenance of regulatory submissions for medical devices and pharmaceuticals.
• Regulations and Guidelines: Comprehensive understanding of global regulations and guidelines, including FDA, EMA, and ICH, that impact regulatory submissions.
• Electronic Submissions: Principles and best practices for electronic submissions, including eCTD and non-eCTD electronic submissions.
• Quality Management Systems: Overview of quality management systems and their impact on regulatory submissions.
• Lifecycle Management: Strategies for managing the regulatory submissions lifecycle, including post-market surveillance and reporting.
• Risk Management: Understanding of risk management principles and their application to regulatory submissions.
• Data Management: Best practices for managing data to support regulatory submissions, including data integrity and data standards.
• Regulatory Audits and Inspections: Preparation and management of regulatory audits and inspections, including responses to audit observations and inspection findings.
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