Webinar Search Results: 23	Topic: Not Specified	Category: All	Speaker: Charles H. Paul

2026 Edition: AI & Machine Learning for Medical...

2026 Edition: AI & Machine Learning for Medical Devices

Artificial Intelligence (AI) and Machine Learning (ML) are rapidly transforming the medical device industry.

Charles H. Paul

February 20, 2026
60 Minutes
US$149.00
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2026 Edition: Electronic Records - Without the Pain

Electronic records are now at the core of nearly every regulated process within the life-sciences industry manufacturing batch records, laboratory data, deviations, investigations, complaints, training documentation, and clinical data, to name a few.

Charles H. Paul

February 26, 2026
60 Minutes
US$149.00
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2026 Edition: Digital Batch Records

As pharmaceutical and biopharmaceutical manufacturing environments become more automated, digital batch records (DBRs)-often implemented as Electronic Batch Records (EBRs) or Manufacturing Batch Records (MBRs)-are replacing traditional paper documentation.

Charles H. Paul

February 27, 2026
60 Minutes
US$149.00
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AI's Errors May Be Impossible to Eliminate - What T...

AI's Errors May Be Impossible to Eliminate - What That Means for Its Use in the FDA

Artificial Intelligence is transforming how work is performed across FDA-regulated industries. Quality teams are experimenting with AI to draft procedures, summarize deviations, analyze complaint data, prepare training materials, and support inspection readiness.

Charles H. Paul

March 2, 2026
60 Minutes
US$149.00
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AI's Errors May Be Impossible to Eliminate - What T...

AI's Errors May Be Impossible to Eliminate - What That Means for Its Use in Accounting & Finance

Artificial Intelligence is rapidly reshaping accounting and finance operations.

Charles H. Paul

March 5, 2026
60 Minutes
US$149.00
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"If It Isn't Written, It Didn't Happen&quo...

"If It Isn't Written, It Didn't Happen": Building Defensible Evidence Trails - Creating Contemporaneous, Inspection-Ready Documentation That Proves Control

In regulated life sciences environments, documentation is more than a formality - it is proof. Whether demonstrating GMP compliance, validating a system, responding to a deviation, or defending decisions during an inspection, organizations must be able to show objective evidence that activities were performed correctly and at the appropriate time.

Charles H. Paul

March 6, 2026
60 Minutes
US$149.00
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Computer Software Assurance (CSA): Building...

Computer Software Assurance (CSA): Building Risk-Based Validation for AI, SaaS & Digital Tools Moving from Documentation Burden to Evidence of Assurance

Life sciences organizations increasingly depend on digital technologies to manage manufacturing, quality, laboratory, and clinical operations. Cloud platforms, SaaS applications, automation tools, and AI-enabled analytics systems now play critical roles in ensuring product quality and patient safety.

Charles H. Paul

March 9, 2026
60 Minutes
US$149.00
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Cross-Functional Change Control: Getting QA, Ops, a...

Cross-Functional Change Control: Getting QA, Ops, and IT Aligned - Streamlining Decisions Without Sacrificing Compliance

Change is constant in regulated life sciences environments. Equipment upgrades, process improvements, software updates, supplier changes, and corrective actions all require formal change control to ensure quality and compliance are maintained.

Charles H. Paul

March 13, 2026
60 Minutes
US$149.00
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Documentation During Crisis: Recalls, OOS Events, a...

Documentation During Crisis: Recalls, OOS Events, and Emergency Changes

In regulated life sciences environments, documentation is always important - but during a crisis, it becomes critical.

Charles H. Paul

March 16, 2026
60 Minutes
US$149.00
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Managing SMEs: Extracting Technical Knowledge for B...

Managing SMEs: Extracting Technical Knowledge for Better SOPs & Reports

In regulated life sciences environments, procedures, reports, and technical documents form the foundation of compliance. Standard operating procedures, validation protocols, investigation reports, and work instructions must accurately describe how work is performed and provide clear, repeatable guidance to those executing tasks.

Charles H. Paul

March 18, 2026
60 Minutes
US$149.00
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Metrics That Predict FDA Findings (Before FDA Does&...

Metrics That Predict FDA Findings (Before FDA Does) - Using Leading Indicators to Detect Risk and Demonstrate Control

Regulatory inspections rarely uncover problems that appear overnight. Most findings - whether related to deviations, CAPAs, training, or documentation - develop gradually over time. Backlogs grow, investigations age, training gaps widen, and recurring issues quietly signal that the quality system is under stress.

Charles H. Paul