This Quality Management System training will discuss how to choose an advanced and comprehensive system for quality and compliance management to meet the unique needs of the FDA-regulated environment.
Insights for quality and compliance managers looking to replacing their point solutions and paper-based systems with an enterprise solution to automate key compliance processes including document control, deviations handling, and CAPA management.
Such systems come apart at their seams as companies grow, resulting in a high risk of non-compliance with cGMP and 21 CFR Part 11 regulations.
Areas Covered in the seminar:
In this Webinar, the presenter will discuss how to choose an advanced and comprehensive system for quality and compliance management to meet the unique needs of the FDA-regulated environment.
It will provide insights to quality and compliance managers looking to replacing their point solutions and paper-based systems with an enterprise solution to
- Automate the quality management processes
- Gain real-time visibility into the quality metrics
- Lower their cost of regulatory compliance
- Reduce the risk of non-compliance.
The Webinar will cover automation requirements of key compliance processes including document control, deviations handling, and CAPA management.
Who Will Benefit
- Quality managers
- Compliance managers
- Regulatory professionals
- Documentation department personnel
- Quality System professionals
- Quality Analyst & executives
- Technical Quality Auditor
- Quality Control / Assurance - Controller
Instructor Profile
Anil Gupta is the Principal of The Applications Marketing Group. He brings over 20 years of experience in marketing enterprise applications, with over half of that in manufacturing and supply chain management. Anil has also consulted with various software and manufacturing companies on planning, materials management, quality management and compliance related issues. Anil has also served as VP of Product Strategy at software companies such as Baan and Niku.
