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

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

CAROLYN TROIANO

October 21 - 22, 2024 | 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

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

Good Manufacturing Practices (GMP) 101

MICHAEL ESPOSITO

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

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

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

GLP Laboratory Compliance Documentation and Recordkeeping

Dr. JOHN C. FETZER

September 05 - 06, 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

Writing SOP’s and Work Instructions that Really Work

CHARLES H. PAUL

September 12 - 13, 2024 | US Eastern Time: 11 AM to 3 PM | Central Europe Time: 5 PM to 9 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

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

Internal and External / Supplier Audits Essentials

JOHN E. LINCOLN

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

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

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

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