Highlights From ISPE Knowledge Network
Explore webinars, training PE articles, and more relevant to your job function.
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Facilities & Equipment
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- 2025 ISPE FOYA Category Winner for Social Impact, Unmet Medical Needs - Berkeley
- Meet the 2025 ISPE FOYA Honorable Mention Award Winner: Erbe Elektromedizin GmbH
- Learn About the Future of USP Plastics in Biotech
- Meet the 2025 ISPE Facility of the Year Awards (FOYA) Category Winner for Pharma 4.0™
Information Systems
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- Digital Validation Mastery: Enabling Validation 4.0
- New GAMP®Guide Provides Framework to Acheive High-Quality AI-Enabled Computerized Systems for Life Sciences
- 2025 ISPE Annual Meeting and Expo Insights from the Executive Chair
- Validation in Transition: Why 2025 is the Turning Point for the Industry
Management
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- 2025 ISPE Annual Meeting and Expo Insights from the Executive Chair
- ISPE Hands-On Biopharmaceutical Manufacturing Facilities and Processes Training
- ISPE Hands-On Controlled Production of Drug Substance and Drug Product in Biomanufacturing
- Using Capacitance as a Process Analytical Technology (PAT) Tool to Improve Productivity and Reduce COGS in Bioprocesses
Product Development
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Quality
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Regulatory
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- The Power of a United Voice: How ISPE Members Can Help Shape Regulatory Guidance
- Navigating Global Oversight USFDA Update: 2025 ISPE China Conference in Shanghai
- Shaping Tomorrow's Pharmaceutical Framework: Embracing Digital Transformation and Technology in an Evolving Landscape
- Navigating through Advanced Therapy Medicinal Products (ATMPs) Guidance and Regulations
Facilities & Equipment
Information Systems
Management
Product Development
Quality
Regulatory
Supply Chain
- 2025 ISPE FOYA Category Winner for Social Impact, Unmet Medical Needs - Berkeley
- Meet the 2025 ISPE FOYA Honorable Mention Award Winner: Erbe Elektromedizin GmbH
- Learn About the Future of USP Plastics in Biotech
- Meet the 2025 ISPE Facility of the Year Awards (FOYA) Category Winner for Pharma 4.0™
- Digital Validation Mastery: Enabling Validation 4.0
- New GAMP®Guide Provides Framework to Acheive High-Quality AI-Enabled Computerized Systems for Life Sciences
- 2025 ISPE Annual Meeting and Expo Insights from the Executive Chair
- Validation in Transition: Why 2025 is the Turning Point for the Industry
- 2025 ISPE Annual Meeting and Expo Insights from the Executive Chair
- ISPE Hands-On Biopharmaceutical Manufacturing Facilities and Processes Training
- ISPE Hands-On Controlled Production of Drug Substance and Drug Product in Biomanufacturing
- Using Capacitance as a Process Analytical Technology (PAT) Tool to Improve Productivity and Reduce COGS in Bioprocesses
- 2025 ISPE Annual Meeting and Expo Insights from the Executive Chair
- ISPE Hands-On Controlled Production of Drug Substance and Drug Product in Biomanufacturing
- Pharma 4.0™ in Progress: How Far Has the Industry Come?
- The Future of ATMPs Pt. 2
- Digital Validation Mastery: Enabling Validation 4.0
- 2025 ISPE Annual Meeting and Expo Insights from the Executive Chair
- Driving Better Outcomes for Quality Control Labs
- Hands-On Aseptic Processing & Annex 1
- The Power of a United Voice: How ISPE Members Can Help Shape Regulatory Guidance
- Navigating Global Oversight USFDA Update: 2025 ISPE China Conference in Shanghai
- Shaping Tomorrow's Pharmaceutical Framework: Embracing Digital Transformation and Technology in an Evolving Landscape
- Navigating through Advanced Therapy Medicinal Products (ATMPs) Guidance and Regulations
Conferences
Webinars
Upcoming
On-Demand
Future-Proofing Pharma & Personal Care: How Life Cycle Assessments & Carbon Footprinting Drive Real Change
Future-Proofing Pharma & Personal Care: How Life Cycle Assessments & Carbon Footprinting Drive Real…
Safer Systems, Smarter Teams: Delivering Just Culture Through Strategic Project Execution
Safer Systems, Smarter Teams: Delivering Just Culture Through Strategic Project Execution…
Sustainable Structural Strategies for Pharma Facilities: Resilience, Compliance, and Innovation
Sustainable Structural Strategies for Pharma Facilities: Resilience, Compliance, and Innovation…
Risk to Regulatory Readiness: A Modern Guide to Sterile Compounding Compliance
Risk to Regulatory Readiness: A Modern Guide to Sterile Compounding Compliance Complimentary…
Unlocking Innovation: Embracing Validation 4.0 for a Digital Pharma Future
Unlocking Innovation: Embracing Validation 4.0 for a Digital Pharma Future Complimentary Learning…
Critical Quality Attributes - Validation of a Parts Washer and Autoclave
Critical Quality Attributes - Validation of a Parts Washer and Autoclave Complimentary Learning…
How Standardized Documentation Drives Compliance, Audit and AI Readiness
How Standardized Documentation Drives Compliance, Audit and AI Readiness Complimentary Learning…
Case Study: Pharma 4.0 Transformation Office
Case Study: Pharma 4.0 Transformation Office Complimentary Learning Level: Intermediate Time: 1000 -…
Transforming Pharmaceutical Supply Planning: A Real-World Implementation of Mathematical Optimization
Transforming Pharmaceutical Supply Planning: A Real-World Implementation of Mathematical…
The Use of Quality Risk Management to Support Commissioning & Qualification - System Risk Assessment
The Use of Quality Risk Management to Support Commissioning & Qualification - System Risk Assessment…
The Future of USP Plastics in Biotech
The Future of USP Plastics in Biotech Complimentary Learning Level: Basic Time: 1100 - 1200 ET…
Future-Proofing Pharma & Personal Care: How Life Cycle Assessments & Carbon Footprinting Drive Real Change
Future-Proofing Pharma & Personal Care: How Life Cycle Assessments & Carbon Footprinting Drive Real…
Safer Systems, Smarter Teams: Delivering Just Culture Through Strategic Project Execution
Safer Systems, Smarter Teams: Delivering Just Culture Through Strategic Project Execution…
Sustainable Structural Strategies for Pharma Facilities: Resilience, Compliance, and Innovation
Sustainable Structural Strategies for Pharma Facilities: Resilience, Compliance, and Innovation…
Risk to Regulatory Readiness: A Modern Guide to Sterile Compounding Compliance
Risk to Regulatory Readiness: A Modern Guide to Sterile Compounding Compliance Complimentary…
Unlocking Innovation: Embracing Validation 4.0 for a Digital Pharma Future
Unlocking Innovation: Embracing Validation 4.0 for a Digital Pharma Future Complimentary Learning…
Critical Quality Attributes - Validation of a Parts Washer and Autoclave
Critical Quality Attributes - Validation of a Parts Washer and Autoclave Complimentary Learning…
How Standardized Documentation Drives Compliance, Audit and AI Readiness
How Standardized Documentation Drives Compliance, Audit and AI Readiness Complimentary Learning…
Case Study: Pharma 4.0 Transformation Office
Case Study: Pharma 4.0 Transformation Office Complimentary Learning Level: Intermediate Time: 1000 -…
Transforming Pharmaceutical Supply Planning: A Real-World Implementation of Mathematical Optimization
Transforming Pharmaceutical Supply Planning: A Real-World Implementation of Mathematical…
The Use of Quality Risk Management to Support Commissioning & Qualification - System Risk Assessment
The Use of Quality Risk Management to Support Commissioning & Qualification - System Risk Assessment…
Introduction to the 2nd Edition of the GAMP GPG on GCP Systems
Introduction to the 2nd Edition of the GAMP GPG on GCP Systems Complimentary Learning Level…
Advancing Aseptic Processing: The Future of Flexible Solutions and Robotics in Pharma Manufacturing
Advancing Aseptic Processing: The Future of Flexible Solutions and Robotics in Pharma Manufacturing…
Improving Productivity and Reducing COGS in Bioprocesses Using Capacitance as a PAT Tool
Improving Productivity and Reducing COGS in Bioprocesses Using Capacitance as a PAT Tool…
Validation in Transition: 2025’s Top Trends, Tools, and Takeaways
Validation in Transition: 2025’s Top Trends, Tools, and Takeaways Sponsored Learning Level…
QRM Based Integrated C&Q Series—System Boundaries and System Classification
QRM Based Integrated C&Q Series—System Boundaries and System Classification Complimentary Learning…
Life Cycle Approach to Process Validation- Stage 3 Implementation
Life Cycle Approach to Process Validation- Stage 3 Implementation Complimentary Learning Level…
Improving Productivity and Reducing COGS in Bioprocesses Using Capacitance as a PAT Tool
ISPE Clinical Supply Business Continuity Survey Results and Discussion Complimentary Learning Level…
Sterilizing-grade Filter Validation
Sterilizing-grade Filter Validation Complimentary Learning Level: Advanced Session Length: 1 hour…
Quality Risk Management Commissioning & Qualification: Key Deliverables & Lessons Learned Webinar
Quality Risk Management Commissioning & Qualification: Key Deliverables & Lessons Learned Webinar…
How to Perform a Compliant Human Error Investigation
How to Perform a Compliant Human Error Investigation Complimentary Learning Level: Advanced Session…
Effective Process Validation Strategies for Successful Product Commercialization
Effective Process Validation Strategies for Successful Product Commercialization Complimentary…
Real Life Case Studies featuring ML/AI including Predictive Maintenance, Defect Detection, Environment
Real Life Case Studies featuring ML/AI including Predictive Maintenance, Defect Detection…
Introduction to the 2nd Edition of the GAMP GPG on GCP Systems
Introduction to the 2nd Edition of the GAMP GPG on GCP Systems Complimentary Learning Level…
Advancing Aseptic Processing: The Future of Flexible Solutions and Robotics in Pharma Manufacturing
Advancing Aseptic Processing: The Future of Flexible Solutions and Robotics in Pharma Manufacturing…
Improving Productivity and Reducing COGS in Bioprocesses Using Capacitance as a PAT Tool
Improving Productivity and Reducing COGS in Bioprocesses Using Capacitance as a PAT Tool…
Validation in Transition: 2025’s Top Trends, Tools, and Takeaways
Validation in Transition: 2025’s Top Trends, Tools, and Takeaways Sponsored Learning Level…
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Industry News
Latest
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ISPE Webinar: Critical Quality Attributes--Validation of a Parts Washer and Autoclave, 27 August
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Identifying Out-of-Trend Data in Stability Studies
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Advancements in Bioprinting Enable Creation of Organ-like Tissues
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Catalent Downsizes at Md. Plant
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Thermo Fisher Acquiring Solventum Filtration Business
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A Look Inside Fujifilm's Plant in N.C.
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J&J Investing $2B in N.C. Manufacturing Capacity
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Computational Model Predicts Solubility in Different Solvents
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Continuous Biomanufacturing is Primed for Success
- Study: Most US Drug Plants in Path of Disaster
Community Discussions
Community Discussions
Aug 22, 2025
Information Systems
Quality
Active Pharmaceutical Ingredients
Biotechnology
Aug 20, 2025
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Quality Assurance
Aug 11, 2025
Quality
Lifecycle Management
Validation
Jul 25, 2025
Data Integrity
Latest Magazine Issue
The AI Paradox Cover: The increasing digitalization of the pharmaceutical and medical device industry has created novel cybersecurity challenges, particularly with the rapid advancement of artificial intelligence (AI)...