Event Catalog

Browse 71 professional development events

Live Webinars33Recorded Webinars37Past Webinars
9 results
IQ, OQ & PQ in 2026: What Now Counts as Sufficient Validation Evidence
Live WebinarNew
Regulatory & ComplianceCertificate

IQ, OQ & PQ in 2026: What Now Counts as Sufficient Validation Evidence

Understand what constitutes sufficient and defensible IQ, OQ, PQ, and PPQ validation evidence in modern GMP environments — with real-world examples.

Meredith CrabtreeMeredith Crabtree
1.5 hoursJun 25, 2026
4.8
$190.00
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Risk-Based CSV/CSA for Modern GxP Systems: Making Defensible Validation Decisions in Practice
Virtual SeminarNew
Computer System ValidationCertificate

Risk-Based CSV/CSA for Modern GxP Systems: Making Defensible Validation Decisions in Practice

A two-day, risk-based framework for CSV/CSA and GAMP® 5 validation decisions on modern GxP systems — cloud, SaaS, configurable, and AI-enabled platforms — built for inspection readiness.

Carolyn TroianoCarolyn Troiano
3 hours/day (2-day course)Sep 10, 2026
4.8
$645.00
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Risk-based Excel Spreadsheet Validation - 2026 Updates
Live WebinarNew
Computer System ValidationCertificate

Risk-based Excel Spreadsheet Validation - 2026 Updates

Master risk-based Excel spreadsheet validation for FDA-regulated environments — covering GAMP 5, SDLC, 21 CFR Part 11, data integrity, and inspection readiness.

Carolyn TroianoCarolyn Troiano
90 minutesSep 4, 2026
4.8
$240.00
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CSA in Practice: How to Build Defensible Evidence the FDA Actually Wants to See
Recorded WebinarNew
Regulatory & ComplianceCertificate

CSA in Practice: How to Build Defensible Evidence the FDA Actually Wants to See

Break through CSV conditioning — learn how to build FDA-defensible evidence using CSA, size effort with risk-based thinking, and align with GAMP 5 (2nd Edition) without the paperwork burden.

Carolyn TroianoCarolyn Troiano
1.5 hours
4.9
$450.00
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FDA Inspection Readiness: Building a Defensible State of Control Before the Investigator Arrives
Recorded WebinarNew
Regulatory & ComplianceCertificate

FDA Inspection Readiness: Building a Defensible State of Control Before the Investigator Arrives

Understand how FDA selects inspection targets, evaluates quality systems remotely, and build a continuous state of control aligned with 21 CFR regulations before the investigator arrives.

Charles H. PaulCharles H. Paul
1.5 hours
4.9
$398.00
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Risk-Based Excel Spreadsheet Validation
Recorded WebinarNew
Regulatory & ComplianceCertificate

Risk-Based Excel Spreadsheet Validation

Apply SDLC, GAMP 5, and risk-based validation to Excel spreadsheets used in FDA-regulated activities — covering Part 11, data integrity, and inspection preparation.

Carolyn TroianoCarolyn Troiano
1.5 hours
4.8
$450.00
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Deviation Backlog Reduction: Balancing Investigation Depth, Closure Speed, and Justifiable Decisions
Live WebinarNew
Regulatory & ComplianceCertificate

Deviation Backlog Reduction: Balancing Investigation Depth, Closure Speed, and Justifiable Decisions

Practical strategies for reducing pharmaceutical deviation backlogs without sacrificing investigation quality — covering risk-based depth, defensible closure, CAPA, and inspection readiness.

Charles H. PaulCharles H. Paul
1 hourAug 27, 2026
4.8
$190.00
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Acceptance Criteria for AI Validation: Determining What "Reliable" Actually Means in GxP Systems
Live WebinarNew
Regulatory & ComplianceCertificate

Acceptance Criteria for AI Validation: Determining What "Reliable" Actually Means in GxP Systems

Learn how to define meaningful, risk-based acceptance criteria for AI systems in GxP environments — covering reliability thresholds, hallucination controls, human guardrails, and CSA-aligned validation strategies.

Carolyn TroianoCarolyn Troiano
1.5 hoursAug 10, 2026
4.8
$240.00
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Audit Trail Review by Exception: Reducing Reviewer Burden Without Weakening Detection
Live WebinarNew
Regulatory & ComplianceCertificate

Audit Trail Review by Exception: Reducing Reviewer Burden Without Weakening Detection

Learn how to implement a risk-based audit trail review-by-exception strategy that reduces reviewer fatigue while strengthening detection of critical compliance, data integrity, and cybersecurity risks.

Carolyn TroianoCarolyn Troiano
1.5 hoursJul 23, 2026
4.8
$240.00
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