Seminars - Eventura

FDA Regulatory Quality Compliance Seminars Workshops and Conferences

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

Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities

CAROLYN TROIANO

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

FDA Inspections and Audit Readiness Course

CHARLES H. PAUL

March 13 - 14, 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

March 20 - 21, 2025 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

Internal and External / Supplier Audits Essentials

JOHN E. LINCOLN

March 24 - 25, 2025 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

Performance of Root Cause Analysis, CAPA, and Effectiveness Checks

MEREDITH CRABTREE

March 27 - 28, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

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

CAROLYN TROIANO

April 03 - 04, 2025 | US Eastern Time: 10 AM to 3 PM | Central Europe Time: 4 PM to 9 PM

FDA Inspections - Top FDA 483 Observations and Prevention Strategies

MEREDITH CRABTREE

April 15 - 16, 2025 | US Eastern Time: 9 AM to 2 PM | Central Europe Time: 3 PM to 8 PM

Technical Writing Excellence in the Life Sciences - A Masterclass

CHARLES H. PAUL

April 24 - 25, 2025 | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 PM

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

JOHN E. LINCOLN

May 13 - 14, 2025 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

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

CHARLES H. PAUL

May 19 - 20, 2025 | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 PM

Bottlenecks to Flow: Optimizing Design Controls and Validation in Medical Device QMS

June 19 - 20, 2025 | US Eastern Time: 10 AM to 4 PM | Central Europe Time: 4 PM to 10 PM

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

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

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

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

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

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

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

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

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

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

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

Live In Person Seminar on Implementing CSA for GxP Systems - Transition, Documentation, and Post-Transition Challenges and Opportunities

CAROLYN TROIANO

February 24 -25, 2025 | Location: Richmond, VA, USA 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

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