Recorded Seminars - Eventura

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

2-Day Seminar Recording

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

MICHAEL ESPOSITO

2-Day Seminar Recording

Computer System Validation For Cloud and Cots Applications

CAROLYN TROIANO

Duration: 6 Hours

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

2-Day Seminar Recording | Course Director: JOY MCELROY

Audit Like the FDA - Effective Internal Audit Program

2-Day Seminar Recording | Course Director: SUSANNE MANZ

Quality Control Laboratory Compliance - cGMP and GLP Training

2-Day Seminar Recording | Course Director: KELLY THOMAS

CSV Boot Camp - 3-Day Certification Course

3-Day Seminar Recording | Course Director: CAROLYN TROIANO

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

CAROLYN TROIANO

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

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

Faculty: SUNDEEP AGARWAL | 2-Part Interactive Webinar Series

Technical Writing Masterclass in the Life Sciences

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

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

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

FDA Inspection Essentials

Duration: 2 DAYS | Course Director: Danielle DeLucy

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

Duration: 6 Hours | Course Director: HITENDRAKUMAR SHAH