Understanding Computer System Validation requirements as per revised Schedule M
Автор: Pharma Best Practices Webinars
Загружено: 2024-05-15
Просмотров: 4952
About the Webinar
With the recent notification of Revised Schedule M by CDSCO, ensuring product quality and compliance has become more critical than ever. Computer Systems are playing a critical role in the pharmaceutical operations. To help you navigate these changes on the Computer Systems Compliance in Schedule M, Pharma Best Practices Foundation is proud to present this webinar covering key aspects of the CSV requirements and best practices for documentation.
About Speaker
Sharmila Valleru is a Director in PwC India, leading the CSV Practice. She is a Subject Matter Expert and a Senior Quality and Regulatory Compliance with more than two decades of experience. She has been assisting Pharma & Lifesciences and Medical Devices companies in the areas of CSV, GxP and IT Compliance. She had assisted both domestic and international companies in the Audits / Gap assessments, Remediations, Training, Automation & Digitalisation.
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