industry speaks: transforming cgmp manufacturing facilities
TRANSCRIPT
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Industry Speaks: Transforming cGMP
Manufacturing Facilities
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Speakers• Principal• DME
David M. Marks, P.E. Speaker/Moderator
• Sr. Director, Engineering, US• Sanofi Pasteur, Inc.
Thomas L. Bryant Discussion Panel
• Associate Director Process Engineering• AstraZeneca Biologics
Robert TorregrossaDiscussion Panel
• Director of Global Engineering PM• Teva Pharmaceuticals
Jeffrey KratzDiscussion Panel
• Director Global Engineering Technology• Biogen
Rich Meinel Discussion Panel
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• An INTERPHEX 2016 Technical Education Program. • Surveys
– Invited engineers, manufacturers, and other life sciences professionals like you to express views on the latest trends and technologies affecting our industry.
– Two Surveys, executed Q4 2015.• Biopharma Facility Modernization• Aseptic Manufacturing Tech Trends
• Whitepapers, issued April 2016.• Presentations with Distinguished Industry Panels.
• Industry Speaks: Transforming cGMP Manufacturing Facilities• Trending Technologies in Sterile Product Manufacturing Facilities
About DME Facility Focus
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Survey Overview
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Survey ParticipantsAFFILIATION JOB FUNCTION
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Triggers & Drivers: When Biomanufacturing Facility
Transformation Becomes a Necessity
6
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Why Change?
Manufacturing ModernizationObsolescence
Reliability
Sustainability
SafetyThroughput
Flexibility
ROI/COGS
Quality
Regulatory Compliance
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Project Drivers
Manufacturing Modernization
Risk Drivers• Product Quality• Regulatory Compliance• Obsolescence• Safety• Reliability
Opportunity Drivers• New Products• Throughput• Flexibility• Sustainability• ROI/COGS
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Opportunity Drivers
1
2
3
4
5
Ranked 1-51 = most frequent
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Risk Drivers
1
2
3
4
5
Ranked 1-51 = most frequent
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cGMP Assessment
Regulatory Audit Findings (e.g. 483 observations, warning letter)
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Equipment Obsolescence
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Biting the Bullet: Committing to a Facility Renovation Project
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Risk FactorsRank the risk factors associated with GMP facility renovations. (Ranked 1 - 5, where 1 = most risk)
1. Legacy facility unknowns; lack of reliable as-built design documentation.
2. Process validation and/or regulatory issues.
3. Impact of renovation on facility segregation and flows.
4. Upgrading equipment to address obsolescence or cGMP gaps.
5. Construction activities adjacent to GMP operations.
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Renovation Risk Factors
1
2 3
4
5
Ranked 1-51 = most frequent
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Risk Assessment
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Enablers: Technologies and Trends that
Provide the Best Modernization Solutions
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New Technologies
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Obstacles to New Technology
IndustryConservatism
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SU Technology Challenges
Operator Training; SS to SU MindsetWarehouse Space; Waste Disposal
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Facility Flexibility
1
2
3
4
5
Ranked 1-51 = most valuable
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Summary
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Transforming Facilities
• Market & Business Drivers• Regulatory Requirements• Disruptive Technologies
The Challenges
Ahead
• Renovations Revisited• Flexible Manufacturing• What’s Next?
The Solutions We Need
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For More Information• Attend our next DME Facility Focus session!
– Trending Technologies in Sterile Product Manufacturing Facilities
– Tuesday, April 26, 1:00-2:00pm, Meeting Room 1• Acquire DME Facility Focus survey whitepapers!
– Available at INTERPHEX: DME booth #1666– Available at www.dmeforlife.com/about-us/facility-focus
after INTERPHEX.• Contact Information
– David M. Marks, PE– [email protected]