Recorded Seminars - Eventura

OOS and OOT Investigations Course - Best Practices, Key Components and a Comprehensive Review of the FDA Requirements

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

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

CHARLES H. PAUL

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

The DHF, Technical Documentation - Similarities, Differences and the Future

JOHN E. LINCOLN

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

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 Completed | Recording and Pre-Registration Available

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

Faculty: SUNDEEP AGARWAL | 2-Part Interactive Webinar Series

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

Duration: 6 Hours | Course Director: HITENDRAKUMAR SHAH

FDA Inspection Essentials

Duration: 2 DAYS | Course Director: Danielle DeLucy

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

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

CSV vs CSA - Waterfall vs. Agile Methodology, Documentation and Implementation

CAROLYN TROIANO

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

Quality Control Laboratory Compliance - cGMP and GLP Training

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

Statistics for Process Control

ELAINE EISENBEISZ

6-Hour Seminar Completed | Recording and Pre-Registration Available

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

CAROLYN TROIANO

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

Analytical Instrument Qualification & Validation – Use of Excel and FDA Audit Preparation

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

Audit Like the FDA - Effective Internal Audit Program

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

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

JOHN E. LINCOLN

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

Biostatistics for the Non-Statistician Training Course

ELAINE EISENBEISZ

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

Technical Writing Excellence in the Life Sciences - A Masterclass

CHARLES H. PAUL

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