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Revised Schedule M: Quality Risk Management (QRM)

999 1,499

Description

“Quality Risk Management (QRM) is a proactive process that identifies, assesses, and mitigates potential risks to ensure pharmaceutical quality, patient safety, and regulatory compliance. Effective QRM strategies leverage risk assessment tools, failure mode and effects analysis (FMEA), and risk-based thinking to minimize errors, optimize processes, and enhance product quality. By integrating QRM into your quality management system, you can reduce risk, improve compliance, and drive business success in the pharmaceutical and medical device industries.”

What I will learn?

  • Improved product quality and patient safety
  • Enhanced regulatory compliance
  • Reduced errors and deviations
  • Increased efficiency and productivity
  • Better decision-making and resource allocation

Course Curriculum

1. Revised Schedule M: Quality Risk Management

  • 1.1 Intro & Keynote Address
    10:46

2. Quality Risk Management

3. Panel Discussion and Open Q & A

4. Closing remarks & Vote of thanks

Session PPT

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999 1,499

Material Includes

  • 4 Learning Videos
  • Course Certificate

Target Audience

  • QA, QC & Manufacturing Professionals

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