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Modernize Risk Assessments by Using Critical Thinking

Tuesday, February 18, 2025
11AM – 12:15PM EST

Presented by Gaurav Walia, Vice President of CSV/CSA/DI & Digital Governance, Head of Chicago PQE Office & Sr. Associate Partner, PQE Group

  • Demonstration of Risk Assessments Concepts
  • Demonstration of Risk Assessments Tools and Strategies
  • Pivoting Away from Traditional Risk Assessments and Encompassing Critical Thinking
  • Pivoting from CSV to CSA with Critical Thinking/Risk Assessment in Mind
  • Real World Highlights of CSA Implementation Case Study with Critical Thinking and Modernized Risk Assessment

Takeaway Tools

  • FDA CSA Draft Guidance (Sep 2022)
  • Article link on Critical Thinking with Modernized Risk Assessment and QdB.
  • Case Study Example of with Critical Thinking and Modernized Risk Assessment

SPEAKERS

Gaurav Walia

VP of CSV/CSA/DI and Digital Governance Head of PQE Chicago Office and Local Equity Partner

  • PQE Group

With over 28 years of experience in the pharmaceutical and medical device industry, I am a passionate and driven leader who strives to deliver excellence in compliance, quality, and regulatory affairs.

As the Vice President of CSV/CSA/DI and Digital Governance and Sr. Associate Partner at PQE Group, I oversee 60+ direct reports globally and provide strategic guidance and solutions for computerized system validation, computer software assurance, and data integrity across various business units and functions.

I have a strong background in laboratory management, technology implementation, software design, budgeting, and international regulatory agencies.

I have successfully designed and managed 200,000+ sq.ft. laboratories, implemented safety and training programs, and handled the entire materials import process for APIs, drugs, intermediates, etc.

I am also an international speaker and trainer for KENX Conferences and Adjunct Lecturervfor Temple University Master’s QA/RA Program and regularly speak and/or attend conferences for PDA, ISPE, ASQ, Institute of Validation Technology, etc. in sharing my insights and expertise on Emerging Quality, Compliance and Regulatory trends as well as innovative updates on technology, AI, Cybersecurity, investigations/CAPAs with Enterprise , Quality, Laboratory, Packaging , Environmental and Manufacturing systems.

I been a part of Major Consent Decree Projects focusing on CSV/DI and Remediation.

I enjoy collaborating with diverse teams and stakeholders, and empowering them to achieve Augmented Success with Quality, Compliance and Regulatory objectives. Plan to achieve common goals and improve business practices.

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