Seminars - Eventura

FDA Regulatory Quality Compliance Seminars Workshops and Conferences

Supplier And Contract Manufacturer Management

FEBRUARY 2 - 3, 2023 US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Aseptic Processing and Validation Course

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

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

JOHN E. LINCOLN

February 13 - 14, 2023 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

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

CHARLES H. PAUL

February 16 - 17, 2023 | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 PM

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

CAROLYN TROIANO

February 21 - 22, 2023 | US Eastern Time: 10 AM to 2 PM | Central Europe Time: 4 PM to 8 PM

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

March 2 - 3, 2023 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

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

March 6 - 7, 2023 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Annual GMP Master Class 2023

CHARLES H. PAUL

March 15 - 17, 2023 | Duration: 3 Days | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 PM

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

Statistics for Process Control

ELAINE EISENBEISZ

April 13, 2023 | US Eastern Time: 11 AM to 5 PM | Central Europe Time: 5 PM to 11 PM

Biostatistics for the Non-Statistician Training Course

ELAINE EISENBEISZ

June 15 - 16, 2023 | US Eastern Time: 11 AM to 5 PM | Central Europe Time: 5 PM to 11 PM

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

Technical Writing Masterclass in the Life Sciences

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

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

Faculty: SUNDEEP AGARWAL | 2-Part Interactive Webinar Series

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

Risk based approach to GxP Compliant Laboratory Computerized Systems

CAROLYN TROIANO

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

21 CFR Part 11 Compliance for Computer Systems Regulated by FDA

CAROLYN TROIANO

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

Complaint Handling, Medical Device Reporting and Recalls - Post-Market Regulations Training

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

21 CFR Part 11 Data Integrity Training for SaaS/Cloud, EU GDPR - How to Reduce Costs for Compliance

CAROLYN TROIANO

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

GLP Laboratory Compliance Documentation and Recordkeeping

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

Building a Robust Vendor Qualification Program for FDA Regulated Industries

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

A TO Z OF Analytical Method Validation, Verification and Transfer

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

Quality Control Laboratory Compliance - cGMPs and GLPs

PRE-REGISTRATION AVAILABLE If you want to have this training scheduled Live and Exclusively for your company, we will arrange it for you. Pre-Register now and pay only once the training is scheduled on your preferred days. Click on the button below to pre-register

Self Inspection Techniques - Avoid the most common and recent FDA observations

Course Director: CARL PATTERSON