Recorded Seminars

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers

SEM3651

JOHN E. LINCOLN

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

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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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Computer System Validation For Cloud and Cots Applications

FDB3540

CAROLYN TROIANO

Duration: 6 Hours Completed | Recording and Pre-Registration Available

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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

The FDA QMSR and the Key Elements of QSIT cGMP Inspection and Audits for Medical Device Manufacturers

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

Computer System Validation For Cloud and Cots Applications

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