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Pharmaceutical Quality Management - Risk Management and Regulatory Compliance, They are Complementary, Not Incompatible
Presented By ComplianceOnline
Wednesday, June 1st at 10:00am PST
Online sale ends: 06/01/22 at 9:30am PST
online event
6201 America Center Drive Suite 240 San Jose, CA 95002, USA
San Jose, CA 95002
-= series =-
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Areas Covered in the Webinar:

  • Quality and risk management defined
  • The QRM process
  • The core principles and common practices of quality management
  • The risk assessment approach
  • Risk management tools - hazard analysis (PHA), risk evaluation and mitigation (REM), hazard analysis critical control point (HACCP), and FMEA
  • Integrating QRM into your quality system
  • The critical QRM regulations and guidance documents that apply to pharmaceutical manufacturing

Regulations that will be Covered:

  • FDA Guidance for Industry – Q8 Pharmaceutical Development
  • FDA Guidance for Industry – Q9 Quality Risk Management
  • FDA Guidance for Industry – Q10 Pharmaceutical Quality System    
  • Who Will Benefit:

  • Quality Assurance Personnel
  • Quality Control Personnel
  • Supply Chain and Logistics Managers
  • Regulatory Affairs Professionals
  • Process Development Scientists and Management
  • Manufacturing Management and Scientists
  • Auditors
  • R&D Management
  • Risk Management Specialists
  • Manufacturing Directors and Supervisors
  • Validation Specialists, Scientists

Presented By

10:00am to 11:30am
Doors open at 9:30am

General Admission: $249.00

online event<br> 6201 America Center Drive Suite 240 San Jose, CA 95002, USA<br> San Jose, 95002



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