ISPE Highlights
iSpeak Blog
ISPE Member Spotlight: Lindsey Daniel
iSpeak Blog
Pharmaceutical Compounding: A US FDA Perspective
iSpeak Blog
ISPE Member Spotlight: Lindsey Daniel
iSpeak Blog
Pharmaceutical Compounding: A US FDA Perspective
Pharmaceutical Engineering Magazine
Guidance Documents
Highlights From ISPE Knowledge Network
Explore webinars, training PE articles, and more relevant to your job function.
These top focus areas bring the most relevant ISPE content to the forefront of your browsing experience. Explore webinars, training, PE articles and more.
Facilities & Equipment
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- Process Architecture and Integrated Design in the Pharmaceutical Sector
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
Information Systems
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- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- The Importance of GAMP® in the Pharmaceutical Industry
- Data Management Requirements for Sterile Manufacturing
- From the Sidelines to the Field: Career Growth Through Industry Engagement
Management
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- Process Architecture and Integrated Design in the Pharmaceutical Sector
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- Elevating Pharmaceutical Quality: Insights from the FDA’s Office of Quality Surveillance and ISPE’s APQ Program
- From the Sidelines to the Field: Career Growth Through Industry Engagement
Product Development
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- Indian Pharmaceutical Industry: Creating Global Impact
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
Quality
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- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- Elevating Pharmaceutical Quality: Insights from the FDA’s Office of Quality Surveillance and ISPE’s APQ Program
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
Regulatory
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- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- Pharmaceutical Compounding: A US FDA Perspective
- Approaches to Lifecycle Management and Regulatory Readiness in Advanced Therapies
- Data Management Requirements for Sterile Manufacturing
Supply Chain
+
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
- Unlock Industry Expertise with Free Access to ISPE’s Select Guidance Documents: A Key Membership Benefit
Facilities & Equipment
Information Systems
Management
Product Development
Quality
Regulatory
Supply Chain
- Process Architecture and Integrated Design in the Pharmaceutical Sector
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- The Importance of GAMP® in the Pharmaceutical Industry
- Data Management Requirements for Sterile Manufacturing
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- Process Architecture and Integrated Design in the Pharmaceutical Sector
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- Elevating Pharmaceutical Quality: Insights from the FDA’s Office of Quality Surveillance and ISPE’s APQ Program
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- Indian Pharmaceutical Industry: Creating Global Impact
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- Elevating Pharmaceutical Quality: Insights from the FDA’s Office of Quality Surveillance and ISPE’s APQ Program
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- Pharmaceutical Compounding: A US FDA Perspective
- Approaches to Lifecycle Management and Regulatory Readiness in Advanced Therapies
- Data Management Requirements for Sterile Manufacturing
- Announcing Pharma 4.0™ and Digitalization Transformation Track at the 2025 ISPE Europe Annual Conference in London, United Kingdom
- From the Sidelines to the Field: Career Growth Through Industry Engagement
- ISPE Members: Optimize Your Membership Experience with ISPE Engage
- Unlock Industry Expertise with Free Access to ISPE’s Select Guidance Documents: A Key Membership Benefit
Conferences
Webinars
Upcoming
On-Demand
Complimentary Member Orientation and Benefits Webinar
Complimentary Member Orientation and Benefits Webinar Complimentary Learning Level: Basic Time: 0900…
Navigating the PFAS Challenge in Pharma: Regulatory Landscape, Risk Management, and Health Implications
Navigating the PFAS Challenge in Pharma: Regulatory Landscape, Risk Management, and Health…
AI/ML in Regulated Life Sciences (GxP) Sectors – Operation Phase: Maintaining a State of Control
AI/ML in Regulated Life Sciences (GxP) Sectors – Operation Phase: Maintaining a State of Control…
Disruptive Medicine Innovation: Next Generation of Combination Product Technologies
Disruptive Medicine Innovation: Next Generation of Combination Product Technologies Complimentary…
How to Perform a Compliant Human Error Investigation
Complimentary Learning Level: Advanced Time: 1100 - 1230 EDT Session Length: 1.5 hour Human error…
Automation Isn’t Automatic: Strategy for Designing and Building a Fully Autonomous Laboratory
Automation Isn’t Automatic: Strategy for Designing and Building a Fully Autonomous Laboratory…
Complimentary Member Orientation and Benefits Webinar
Complimentary Member Orientation and Benefits Webinar Complimentary Learning Level: Basic Time: 0900…
Navigating the PFAS Challenge in Pharma: Regulatory Landscape, Risk Management, and Health Implications
Navigating the PFAS Challenge in Pharma: Regulatory Landscape, Risk Management, and Health…
AI/ML in Regulated Life Sciences (GxP) Sectors – Operation Phase: Maintaining a State of Control
AI/ML in Regulated Life Sciences (GxP) Sectors – Operation Phase: Maintaining a State of Control…
Disruptive Medicine Innovation: Next Generation of Combination Product Technologies
Disruptive Medicine Innovation: Next Generation of Combination Product Technologies Complimentary…
How to Perform a Compliant Human Error Investigation
Complimentary Learning Level: Advanced Time: 1100 - 1230 EDT Session Length: 1.5 hour Human error…
Automation Isn’t Automatic: Strategy for Designing and Building a Fully Autonomous Laboratory
Automation Isn’t Automatic: Strategy for Designing and Building a Fully Autonomous Laboratory…
Complimentary Member Orientation and Benefits Webinar
Complimentary Member Orientation and Benefits Webinar Complimentary Learning Level: Basic Time: 0900…
Navigating the PFAS Challenge in Pharma: Regulatory Landscape, Risk Management, and Health Implications
Navigating the PFAS Challenge in Pharma: Regulatory Landscape, Risk Management, and Health…
AI/ML in Regulated Life Sciences (GxP) Sectors – Operation Phase: Maintaining a State of Control
AI/ML in Regulated Life Sciences (GxP) Sectors – Operation Phase: Maintaining a State of Control…
Disruptive Medicine Innovation: Next Generation of Combination Product Technologies
Disruptive Medicine Innovation: Next Generation of Combination Product Technologies Complimentary…
Using Simulations to Accelerate Pharmaceutical Manufacturing Processes
Using Simulations to Accelerate Pharmaceutical Manufacturing Processes Extended Learning Learning…
Complimentary Member Orientation and Benefits Webinar
Complimentary Member Orientation and Benefits Webinar Complimentary Learning Level: Basic Session…
QRM Based Integrated C&Q Series - Implementing a Science and Risk Based Approach to Commissioning & Qualification
QRM Based Integrated C&Q Series - Implementing a Science and Risk Based Approach to Commissioning &…
Holistic Pharma 4.0 Digital Maturity Assessment
Holistic Pharma 4.0 Digital Maturity Assessment Complimentary Learning Level: Basic Session Length…
CSV vs CSA: GAMP 5's Actionable Steps to Transitioning Your Validation
CSV vs CSA: GAMP 5's Actionable Steps to Transitioning Your Validation Complimentary Learning Level…
Actively Identifying Limiting Factors in Speed to Launch Drug Products
Actively Identifying Limiting Factors in Speed to Launch Drug Products Complimentary Learning Level…
Secrets in the Digital Transformation Vibe
Secrets in the Digital Transformation Vibe Powered and Led by Women in Pharma ® This session…
Improved Data Integrity via Digitization of Environmental Monitoring
Improved Data Integrity via Digitization of Environmental Monitoring Complimentary Learning Level…
Purified Water Microbial Testing: False OOS Due to TNTC vs Filtration Volume
Purified Water Microbial Testing: False OOS Due to TNTC vs Filtration Volume Complimentary Learning…
Quality Culture Matters: Key to Unlocking the Digital Validation Power
Quality Culture Matters: Key to Unlocking the Digital Validation Power Extended Learning Learning…
Visual Inspection Defects in Oral Solid Dosage Forms: Effective Troubleshooting Strategies
Visual Inspection Defects in Oral Solid Dosage Forms: Effective Troubleshooting Strategies Extended…
Blue Sky Lab Automation for the QC Industry
Blue Sky Lab Automation for the QC Industry Complimentary Learning Level: Advanced Session Length: 1…
Using Simulations to Accelerate Pharmaceutical Manufacturing Processes
Using Simulations to Accelerate Pharmaceutical Manufacturing Processes Extended Learning Learning…
Complimentary Member Orientation and Benefits Webinar
Complimentary Member Orientation and Benefits Webinar Complimentary Learning Level: Basic Session…
QRM Based Integrated C&Q Series - Implementing a Science and Risk Based Approach to Commissioning & Qualification
QRM Based Integrated C&Q Series - Implementing a Science and Risk Based Approach to Commissioning &…
Holistic Pharma 4.0 Digital Maturity Assessment
Holistic Pharma 4.0 Digital Maturity Assessment Complimentary Learning Level: Basic Session Length…
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Industry News
Latest
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The Importance of GAMP® in the Pharmaceutical Industry
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Diverse Case Studies at the 2025 ISPE Aseptic Conference
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MHRA Issues Rule for Decentralized ATMP Production
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ABVC BioPharma to Integrate Botanicals, Pharma Production
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Halo Pharma Facility in N.J. Adds Sterile Filling Line
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Syngene Acquires Emergent Biologics Facility in Md.
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Benefits, Challenges to Retrofitting Buildings for Pharma Production
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Artificial Photosynthesis Converts Waste into Pharmaceuticals
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AI, Automation to Advance Africa's RNA Vaccine Production
- Merck Opens $1B Vaccine Plant in N.C.
Community Discussions
Community Discussions
Feb 16, 2025
Workforce of the Future
Feb 15, 2025
Manufacturing Operations
Feb 13, 2025
Manufacturing Operations
Oral Solid Dosage
Feb 10, 2025
Sustainable Facilities, HVAC, & Controlled Environments
Feb 06, 2025
Latest Magazine Issue
GAMP® is indispensable for safeguarding the safety, quality, and compliance of pharmaceutical products, ultimately benefiting both companies and patients alike. In this issue, we delve into key developments in GAMP...