Recorded Seminars

Data Integrity by Design and Pharma 4.0: Next-Gen Techniques to Approach GxP Systems, and FDA Compliance

SEM3549

CAROLYN TROIANO

2-Day Seminar Completed | Recording and Pre-Registration Available

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The New EU Medical Devices Regulations Training - Essential Tasks to Complete the EU MDR Implementation and Transition

SEM3205

KELLY THOMAS

2-Day Seminar Recording

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Quality and Regulatory pathways for SaMD and AI devices - All you need to know

MD3530

Faculty: SUNDEEP AGARWAL | 2-Part Interactive Webinar Series

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Annual Product Quality Reviews – Preparation, Reports, Impact of Latest Quality Metrics Guidance

ISEM1408

Duration: 6 Hours | Course Director: HITENDRAKUMAR SHAH

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Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA

SEM3544

CAROLYN TROIANO

2-Day Seminar Completed | Recording and Pre-Registration Available

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Audit Like the FDA - Effective Internal Audit Program

SEM3126

SUSANNE MANZ

2-Day Seminar Completed | Recording and Pre-Registration Available

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Process Validation Training Course (FDA and EU Annex 15: Qualifications And Validation)

SEM3570

JOY MCELROY

2-Day Seminar Completed | Recording and Pre-Registration Available

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Aseptic Processing and Validation Course

SEM3206

KELLY THOMAS

2-Day Seminar Completed | Recording and Pre-Registration Available

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Process Validation Requirements and Compliance Strategies (Now in Spanish and English)

MD3046

JOSÉ MORA

Seminar Completed | Recording and Pre-Registration Available

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SOP Synergy 2024

SEM1582

4 Expert Speakers

2-Day Seminar Completed | Recording and Pre-Registration Available

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Biostatistics for the Non-Statistician Training Course

SEM3137

ELAINE EISENBEISZ

2-Day Seminar Completed | Recording and Pre-Registration Available

Recorded Seminars

Effective Internal Audit Program

Human Error Prevention Training - Preventing Active and Latent Error in the Life Sciences

Quality Control Laboratory Compliance - cGMP and GLP Training

A TO Z OF Analytical Method Validation, Verification and Transfer

Effective SOP Writing Masterclass - Training and Compliance in the Pharmaceutical Industry

GMP Auditing of Active Pharmaceutical Ingredients (APIs) and Excipient Suppliers

Annual GMP Master Class 2024

Data Integrity by Design and Pharma 4.0: Next-Gen Techniques to Approach GxP Systems, and FDA Compliance

The New EU Medical Devices Regulations Training - Essential Tasks to Complete the EU MDR Implementation and Transition

Quality and Regulatory pathways for SaMD and AI devices - All you need to know

Annual Product Quality Reviews – Preparation, Reports, Impact of Latest Quality Metrics Guidance

FDA Inspection Essentials

Death by CAPA - Does your CAPA Program need a CAPA?

Statistics for Process Control

Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA

Audit Like the FDA - Effective Internal Audit Program

Process Validation Training Course (FDA and EU Annex 15: Qualifications And Validation)

Aseptic Processing and Validation Course

Process Validation Requirements and Compliance Strategies (Now in Spanish and English)

SOP Synergy 2024

Biostatistics for the Non-Statistician Training Course