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

Developing Effective Post Market Surveillance and Complaint Handling Requirements (Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls)

JOHN E. LINCOLN

December 10 - 11, 2024 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

Validating and Auditing Cloud, SaaS, IaaS, PaaS Systems - Tech & Validation Trends for FDA Compliance

CAROLYN TROIANO

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

Writing SOP’s and Work Instructions that Really Work

CHARLES H. PAUL

January 23 - 24, 2025 | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 PM

GLP Laboratory Compliance Documentation and Recordkeeping

Dr. JOHN C. FETZER

February 06 - 07, 2025 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

SaMD Masterclass - Validation, Change Management, Cybertechnology, and Best Practices

CAROLYN TROIANO

February 10 - 11, 2025 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

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

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

CAROLYN TROIANO

September 23 -24, 2024 | 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

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

Good Manufacturing Practices (GMP) 101

MICHAEL ESPOSITO

March 06 - 07, 2025 | 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

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

Supplier And Contract Manufacturer Management

October 24 - 25, 2024 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Design of Experiments 101 - Methods and Analysis

December 12 - 13, 2024 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

FDA Inspections Seminar for 2024

November 14 - 15, 2024 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

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

CAROLYN TROIANO

September 23 -24, 2024 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Analytical Instrument Qualification and Excel Validation - Preparing for FDA Audits

September 11 - 12, 2024 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

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

JOHN E. LINCOLN

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

Biostatistics for the Non-Statistician Training Course

ELAINE EISENBEISZ

2-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

September 26 - 27, 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

October 15, 2024 | US Eastern Time: 9 AM to 3 PM | Central Europe Time: 3 PM to 9 PM

Effective Internal Audit Program

MEREDITH CRABTREE

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

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

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

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

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

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

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

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

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