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Mr.David Nettleton

What Exactly is Required for 21 CFR Part 11 and Annex 11 Compliance?

Pharmaceutical

Duration: 90 Minutes |
From: Nov 17, 2023 - To: Jan 01, 1970

Dr. Ginette M. Collazo

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

Pharmaceutical

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

Dr. Ginette M. Collazo

Human Error Solutions: How we reduced 60% of human errors in less than a year, a Case Study

Pharmaceutical

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

Dr. Ginette M. Collazo

Reducing memory and attention failures/errors: Understanding Cognitive Load

Pharmaceutical

Duration: 90 Minutes |
From: Jan 11, 2022 - To: Dec 31, 2022

Dr. Ginette M. Collazo

Latest trends And Understanding Human Error. Why people make mistakes?

Pharmaceutical

Duration: 90 Minutes |
From: Nov 30, 2021 - To: Dec 31, 2021

David Nettleton

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Pharmaceutical

Duration: 360 Minutes |
From: Nov 29, 2021 - To: Dec 31, 2021

John E Lincoln

Verification and Validation - Product, Equipment/Process, Software and QMS

Pharmaceutical

Duration: 480 Minutes |
From: Nov 29, 2021 - To: Dec 31, 2021

Dr. Ginette M. Collazo

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

Pharmaceutical

Duration: 60 Minutes |
From: Nov 29, 2021 - To: Dec 31, 2021

Roger Cowan

CMO Supplier Quality Agreements - How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture

Pharmaceutical

Duration: 60 Minutes |
From: Nov 29, 2021 - To: Dec 31, 2021

Cynthia Brysch

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

Pharmaceutical

Duration: 480 Minutes |
From: Nov 28, 2021 - To: Dec 31, 2021

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Pharmaceutical

What Exactly is Required for 21 CFR Part 11 and Annex 11 Compliance?

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

Reducing memory and attention failures/errors: Understanding Cognitive Load

Latest trends And Understanding Human Error. Why people make mistakes?

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Verification and Validation - Product, Equipment/Process, Software and QMS

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

CMO Supplier Quality Agreements - How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

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Pharmaceutical

What Exactly is Required for 21 CFR Part 11 and Annex 11 Compliance?

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

Reducing memory and attention failures/errors: Understanding Cognitive Load

Latest trends And Understanding Human Error. Why people make mistakes?

21 CFR Part 11 Compliance for SaaS/Cloud Applications

Verification and Validation - Product, Equipment/Process, Software and QMS

Human Error and Cognitive Load: How to Reduce Memory and Attention Failures

CMO Supplier Quality Agreements - How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture

PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation

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Speaker Opportunity

Suggest a Topic

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