Complimentary

These webinars are FREE for anyone to register and attend.  Registered attendees receive access to the webinar for 30 days.  After 30 days, ISPE Members have the benefit of unlimited access to the complimentary webinar recordings and presentations - even if you don't sign up for the webinar. So, if you’re not a Member - Join today!

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Exploring the Risk-Knowledge Infinity Cycle (RKI Cycle) Across the Product Lifecycle Webinar

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Complimentary Learning Level: Intermediate Session Length: 1 hour Quality Risk Management (QRM) and Knowledge Management (KM) are positioned as dual enablers to an effective Pharmaceutical Quality System. While there is...
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Women in Pharma: Emphasizing Cognitive Diversity in the Workplace & Beyond Webinar

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Complimentary Learning Level: Intermediate Session Length: 1 hour Cognitive diversity is the inclusion of people who have different ways of thinking, different viewpoints and different skill sets in a team or business...
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Driving Patient Safety, Production Efficiency and Quality in Parenteral Manufacturing through the Use of Container Traceability Webinar

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Complimentary Learning Level: Intermediate Session Length: 60 minutes Health authorities and regulators are increasingly looking for much higher levels traceability during the manufacture of parenteral medicines. The...
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Explore the GAMP Data Integrity by Design Guide Webinar

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Complimentary Learning Level: Intermediate Session Length: 60 minutes Based on the new ISPE GAMP Data Integrity by Design Guide, this webinar will examine the underlying concepts around designing data integrity into your...
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Secrets to Cleaning Validation Success – How to Increase Efficiency with TOC Webinar

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Complimentary Learning Level: Basic/Intermediate How efficient is your cleaning verification or validation monitoring program? How confident are you that your cleaning method adequately removes all degradants and...
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How Digital Technology is Reshaping Assembly Processes for Medical Device Manufacturing Webinar

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Complimentary Learning Level: Advanced Digital Twin, Data-based Quality Control, Performance Dashboards, etc. The era of digitalization has begun, and we just started understanding some of the winnings. The latest...
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A Practical Examination of How to Use Risk Assessments in the CSV Process Webinar

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Complimentary Learning Level: Intermediate Risk Assessments are a core part of regulatory compliance, but many lab organizations struggle to properly scale their Computerized System Validation (CSV) activities based on...
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Where Artificial Intelligence (AI) Fits in the Pharma Value Chain

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Learning Level: Intermediate Over the last several decades, the complexity of the pharmaceutical industry has increased immensely. Today, large pharmaceutical companies deal with higher product volumes, more diverse SKUs...
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Analytical Instrument Qualification – A Continuum of Requirements, from USP <1058> to GAMP® 5 Webinar

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Learning Level: Basic/Intermediate - Analytical laboratories are required to demonstrate the suitability of their equipment during audits and will typically follow USP requirements defined in Chapter 1058> on analytical...
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Bridging the Communication Gap Between Critical Utilities & Regulators: NEW ISPE Critical Utilities GMP Compliance Guide

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Learning Level: Intermediate - Because of their hidden nature, critical utility systems are vulnerable to non-compliance. With their potential to impact product quality or performance in a significant way, critical...