Virtual Seminars

Danielle DeLucy

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

4 Hours
LIVE

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Marina Malikova

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

4 Hours
LIVE

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Joy McElroy

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

4 Hours
LIVE

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Carolyn Troiano

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

4 Hours
LIVE

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Susanne Manz

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

3 Hours
LIVE

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Danielle DeLucy

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

3 Hours
LIVE

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Danielle DeLucy

3-Hour Virtual Seminar on Successful Deviation Investigations

3 Hours
LIVE

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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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Joy McElroy

3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipmen

3 Hours
RECORDED

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Dr. Ronald D. Snee

3 Hours Virtual Seminar on Root Cause Analysis for CAPA Investigations

3 Hours
RECORDED

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José Mora

3-Hour Virtual Seminar on IEC 62304 and Demystifying Software Validation using the Princip

3 Hours
RECORDED

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Michael Esposito

3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: G

3 Hours
RECORDED

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Joy McElroy

4-Hour Virtual Seminar on Good Laboratory Practices (GLPs) vs GMPs – Comparison and

4 Hours
RECORDED

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Kelly Thomas

4-Hours Virtual Seminar on Change Control According to GxP and GMP Requirements

4 Hours
RECORDED

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Carolyn Troiano

4-Hour Virtual Seminar on Computer System Validation (CSV) and Data Integrity for Clinical

4 Hours
RECORDED

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1 2 next »

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

3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipmen

3 Hours Virtual Seminar on Root Cause Analysis for CAPA Investigations

3-Hour Virtual Seminar on IEC 62304 and Demystifying Software Validation using the Princip

3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: G

4-Hour Virtual Seminar on Good Laboratory Practices (GLPs) vs GMPs – Comparison and

4-Hours Virtual Seminar on Change Control According to GxP and GMP Requirements

4-Hour Virtual Seminar on Computer System Validation (CSV) and Data Integrity for Clinical

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