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Carolyn (McKillop) Troiano

Computer System Validation (CSV) and Computer Software Assurance (CSA)

PharmaceuticalDuration: 90 Minutes | From: Feb 14, 2022 - To: Dec 31, 2022

Available

All Days

Ginette Collazo

How To Reduce Human Error Once And For All: Investigations, Root Cause Determination And CAPA Effectiveness

PharmaceuticalDuration: 90 Minutes | From: Feb 10, 2022 - To: Dec 31, 2022

Available

All Days

Ginette Collazo

Human Error Solutions: How We Reduced 60% Of Human Errors In Less Than A Year, A Case Study

PharmaceuticalDuration: 90 Minutes | From: Jan 26, 2022 - To: Dec 31, 2022

Available

All Days

Kelly Thomas

FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

PharmaceuticalDuration: 90 Minutes | From: Jan 10, 2022 - To: Dec 31, 2022

Available

All Days

Peggy J. Berry

Comparability Protocols For Approved Drugs

PharmaceuticalDuration: 90 Minutes | From: Dec 15, 2021 - To: Dec 31, 2021

Available

All Days

David Nettleton

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

PharmaceuticalDuration: 75 Minutes | From: Dec 02, 2021 - To: Dec 31, 2021

Available

All Days

Jose Mora

How to Conduct a Human Factors / Usability Validation

PharmaceuticalDuration: 60 Minutes | From: Nov 30, 2021 - To: Dec 31, 2021

Available

All Days

Michael Levin

Process Analytical Technology (PAT)

PharmaceuticalDuration: 60 Minutes | From: Nov 23, 2021 - To: Dec 31, 2021

Available

All Days

Roger Cowan

Pharmaceutical Compressed Air - Quality GMP Requirements

PharmaceuticalDuration: 60 Minutes | From: Nov 23, 2021 - To: Dec 31, 2021

Available

All Days

Michael Esposito

Packaging and Labeling in Pharmaceutical Product Development – Best Practices

PharmaceuticalDuration: 60 Minutes | From: Nov 02, 2021 - To: Dec 31, 2021

Available

All Days

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Pharmaceutical

Computer System Validation (CSV) and Computer Software Assurance (CSA)

How To Reduce Human Error Once And For All: Investigations, Root Cause Determination And CAPA Effectiveness

Human Error Solutions: How We Reduced 60% Of Human Errors In Less Than A Year, A Case Study

FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

Comparability Protocols For Approved Drugs

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

How to Conduct a Human Factors / Usability Validation

Process Analytical Technology (PAT)

Pharmaceutical Compressed Air - Quality GMP Requirements

Packaging and Labeling in Pharmaceutical Product Development – Best Practices

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Pharmaceutical

Computer System Validation (CSV) and Computer Software Assurance (CSA)

How To Reduce Human Error Once And For All: Investigations, Root Cause Determination And CAPA Effectiveness

Human Error Solutions: How We Reduced 60% Of Human Errors In Less Than A Year, A Case Study

FDA Compliant Handling of Out-of-Trend Results in Pharmaceutical Quality Control

Comparability Protocols For Approved Drugs

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

How to Conduct a Human Factors / Usability Validation

Process Analytical Technology (PAT)

Pharmaceutical Compressed Air - Quality GMP Requirements

Packaging and Labeling in Pharmaceutical Product Development – Best Practices

Un-Subscribe

Speaker Opportunity

Suggest a Topic

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