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Recorded Seminars


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Recording

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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Recording

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

SEM2886
MICHAEL ESPOSITO

2-Day Seminar Recording

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Recording

Computer System Validation For Cloud and Cots Applications

FDB3540
CAROLYN TROIANO

Duration: 6 Hours

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Recording

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

SEM3570

2-Day Seminar Recording | Course Director: JOY MCELROY

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Recording

Audit Like the FDA - Effective Internal Audit Program

SEM3126

2-Day Seminar Recording | Course Director: SUSANNE MANZ

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Recording

Quality Control Laboratory Compliance - cGMP and GLP Training

SEM3204

2-Day Seminar Recording | Course Director: KELLY THOMAS

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Recording

CSV Boot Camp - 3-Day Certification Course

SEM3541

3-Day Seminar Recording | Course Director: CAROLYN TROIANO

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16 - 17 MAR '23

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

SEM3544
CAROLYN TROIANO

March 16 - 17, 2023 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

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Recording

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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Recording

Technical Writing Masterclass in the Life Sciences

SEM3567

2-Day Seminar Recording | Course Director: CHARLES H. PAUL

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Recording

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

SEM3784

2-Day Seminar Recording + Q&A Sessions | Course Director: JOHN E LINCOLN

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Recording

FDA Inspection Essentials

SEM2084

Duration: 2 DAYS | Course Director: Danielle DeLucy

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Recording

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

ISEM1408

Duration: 6 Hours | Course Director: HITENDRAKUMAR SHAH

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