Seminars - Eventura

FDA Regulatory Quality Compliance Seminars Workshops and Conferences

WATCH VIDEO: Project Management for Non-Project Managers - Introduction to training series (MODULE 1)

CHARLES H. PAUL

CLICK ON PLAY BUTTON TO WATCH THE WEBINAR Areas Covered in the Session : What are projects? | The importance of project management. | Projects, programs, portfolios, and operations management. | Benefits of effective project management. | The role of the project manager. | The importance of understanding project initiation. | Project management process. | Introduction to the entire series of modules

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

MICHAEL ESPOSITO

April 29 - 30, 2024 | US Eastern Time: 9 AM to 4 PM | Central Europe Time: 3 PM to 10 PM

A TO Z OF Analytical Method Validation, Verification and Transfer

May 02 - 03, 2024 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 2 PM to 7 PM

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

CHARLES H. PAUL

May 09 - 10, 2024 | 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

May 16 - 17, 2024 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Quality Control Laboratory Compliance - cGMP and GLP Training

May 23 - 24, 2024 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

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

JOHN E. LINCOLN

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

Technical Writing Excellence in the Life Sciences - A Masterclass

CHARLES H. PAUL

June 13 - 14, 2024 | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 PM

Internal and External / Supplier Audits Essentials

JOHN E. LINCOLN

June 24 - 25, 2024 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

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

SOP Synergy 2024

4 Expert Speakers

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

Statistics for Quality Control

ELAINE EISENBEISZ

November 30, 2023 | US Eastern Time: 11 AM to 5 PM | Central Europe Time: 5 PM to 11 PM

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

Seminar Completed | Recording and Pre-Registration Available

Aseptic Processing and Validation Course

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

MedReg 2023 - Annual Medical Device Regulatory Confex

10 Expert Speakers

3-Day Seminar Completed

CSV Boot Camp - 3-Day Certification Course

CAROLYN TROIANO

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

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

Supplier And Contract Manufacturer Management

2-Day Seminar | Recording and Pre-Registration Available

Audit Like the FDA - Effective Internal Audit Program

2-Day 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

Statistics for Process Control

ELAINE EISENBEISZ

6-Hour 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

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

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

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

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

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

CAROLYN TROIANO

April 11 - 12, 2024 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Building a Robust Vendor Qualification Program for FDA Regulated Industries

March 18 - 19, 2024 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Is it a Drug, a Medical Device or both? Determine Product Classification with Precision and Risk

MEREDITH CRABTREE

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

Statistical Elements of Implementing ICH Quality Guidelines

ELAINE EISENBEISZ

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 CSV, CSA, SaaS/Cloud - 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

Medical Device Design Control Essentials Course

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

Enhancing Quality Oversight in Pharmaceutical Contract Manufacturing Organizations

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

Writing and Implementing a Standard Operating Procedure (SOP) in a Compliant Laboratory (US FDA, US EPA and OSHA Focus)

Dr. JOHN C. FETZER

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

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

Project Management for Non-Project Managers - Certification Training Series

CHARLES H. PAUL

October 02 - November 10, 2023 | 15 Modules | 25 Hours US Eastern Time: 11 AM | Central Europe Time: 4 PM

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