Effective Quality by Design (QbD)

Date	Oct 24, 2018
Time	03:00 PM EDT
Cost	$200.00
Online

This webinar will pave a solid path to those who want to ensure making their QbD (Quality by Design) the strongest link in their quality system and see their product launched successfully in the market for patients.

Areas Covered in the Session :

• Unique product design and development requirements
• Major considerations in the regulatory requirements for product design
• Insight into the GMP regulations
• Simplifying the planning and execution phase of your product
• Quality System requirements for your Design Control System
• Emerging medical device and pharma development
• Design Control and manufacturing requirements per ICH Guidelines
• 21 CFR 820, 210/211 and ISO 13485
• Currently available FDA Guidance Documents
• Risk-based Assessment
• Essential component of a well-documented quality system
• Solid identification and documentation of root cause
• What data should you gather for each stage of product development
• Proof of evidence needed by regulators
• How to sustain the life cycle of your medical product

Who Should Attend:

• Manufacturing Departments
• Process Engineering Departments
• Research and Development Departments
• Design Assurance Departments
• Quality Assurance Departments
• Quality Control Departments
• Document Control Departments
• Regulatory Affairs Departments
• QbD Consultants