Virtual Seminars

Charles Paul

3-Hour Virtual Seminar on Technical Training in Life Sciences

3 Hours
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Angela Bazigos

3-Hour Virtual Seminar on Off Label Promotion for Drugs and Medical Devices

3 Hours
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Joy McElroy

3-Hour Virtual Seminar on Effective Cleaning Validation Procedures – Best Practices

3 Hours
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Kelly Thomas

3-Hour Virtual Seminar on Establishing a Robust Data Integrity Program

3 Hours
LIVE

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Edwin Waldbusser

4-Hour Virtual Seminar on Design Control Program with Detailed Hazard Analysis, Human Fact

4 Hours
LIVE

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Angela Bazigos

3-Hour Virtual Seminar on Excel Spreadsheet Validation for FDA 21 CFR Part 11

3 Hours
RECORDED

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Dr. Ginette Collazo

3-Hour Virtual Seminar on Controlling Human Error in Manufacturing Floor

3 Hours
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Danielle DeLucy

4-Hour Virtual Seminar on Batch Record Review and Product Release

4 Hours
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Marina Malikova

4-Hour Virtual Seminar on Preparing and Submitting Investigational New Drug (IND) & I

4 Hours
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Joy McElroy

4-Hour Virtual Seminar on Analytical Instrument Qualification and Validation – Understan

4 Hours
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Carolyn Troiano

4-Hour Virtual Seminar on Risk-Based Approach to Part 11 Compliance and Policies and Proce

4 Hours
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Susanne Manz

3-Hour Virtual Seminar on IQ, OQ, PQ in the Verification and Validation Process

3 Hours
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Danielle DeLucy

3-Hour Virtual Seminar on Aseptic Technique and Cleanroom Behavior – Avoiding Human

3 Hours
RECORDED

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Danielle DeLucy

3-Hour Virtual Seminar on Successful Deviation Investigations

3 Hours
RECORDED

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Carolyn Troiano

4-Hour Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Si

4 Hours
RECORDED

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1 2 3 next »

3-Hour Virtual Seminar on Technical Training in Life Sciences

3-Hour Virtual Seminar on Off Label Promotion for Drugs and Medical Devices

3-Hour Virtual Seminar on Effective Cleaning Validation Procedures – Best Practices

3-Hour Virtual Seminar on Establishing a Robust Data Integrity Program

4-Hour Virtual Seminar on Design Control Program with Detailed Hazard Analysis, Human Fact

3-Hour Virtual Seminar on Excel Spreadsheet Validation for FDA 21 CFR Part 11

3-Hour Virtual Seminar on Controlling Human Error in Manufacturing Floor

4-Hour Virtual Seminar on Batch Record Review and Product Release

4-Hour Virtual Seminar on Preparing and Submitting Investigational New Drug (IND) & I

4-Hour Virtual Seminar on Analytical Instrument Qualification and Validation – Understan

4-Hour Virtual Seminar on Risk-Based Approach to Part 11 Compliance and Policies and Proce

3-Hour Virtual Seminar on IQ, OQ, PQ in the Verification and Validation Process

3-Hour Virtual Seminar on Aseptic Technique and Cleanroom Behavior – Avoiding Human

3-Hour Virtual Seminar on Successful Deviation Investigations

4-Hour Virtual Seminar on 21 CFR Part 11 Guidance for Electronic Records and Electronic Si

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