Recorded Seminars - Eventura

Project Management in the Life Sciences - Project Management Fundamentals for Non-Project Managers

CHARLES H. PAUL

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

Effective Internal Audit Program

MEREDITH CRABTREE

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

Quality Control Laboratory Compliance - cGMP and GLP Training

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

Internal and External / Supplier Audits Essentials

JOHN E. LINCOLN

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

A TO Z OF Analytical Method Validation, Verification and Transfer

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

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

MICHAEL ESPOSITO

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

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

JOHN E. LINCOLN

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

Annual GMP Master Class 2024

CHARLES H. PAUL

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

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

JOHN E. LINCOLN

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

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

CAROLYN TROIANO

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

FDA Inspections and Audit Readiness Course

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

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

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

Audit Like the FDA - Effective Internal Audit Program

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

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

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

Aseptic Processing and Validation Course

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

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

Seminar Completed | Recording and Pre-Registration Available

SOP Synergy 2024

4 Expert Speakers

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