CHARLES H. PAUL - Eventura

4-Hour Virtual Seminar on Project Management for Non-Project Managers

CHARLES H. PAUL

Duration: 4 Hours

3-Hour Virtual Seminar on 510(k) and PMA Submissions Process

CHARLES H. PAUL

Duration: 3 Hours

How FDA trains its Investigators to Review CAPA and How should you prepare

CHARLES H. PAUL

Duration: 60 Minutes

6-Hour Virtual Seminar on Write SOP’s and Work Instructions that Really Work

CHARLES H. PAUL

Duration: 6 Hour

FDA Establishment Inspections – What to Expect

CHARLES H. PAUL

Duration: 60 Minutes

Good Manufacturing Practices – 3 Hour Virtual Seminar

CHARLES H. PAUL

Duration: 3 Hour

510(k) and PMA Refuse to Accept Policy

CHARLES H. PAUL

Duration: 60 Minutes

Medical Device Classifications

CHARLES H. PAUL

Duration: 60 Minutes

Building a Compliant Documentation and Training System

CHARLES H. PAUL

Duration: 60 Minutes

Best Practices in Providing Coaching and Feedback to Team Members

CHARLES H. PAUL

Duration: 90 Minutes

Good Manufacturing Practices for Medical Devices

CHARLES H. PAUL

Duration: 60 Minutes

FDA and EU Medical Device Submissions

CHARLES H. PAUL

Duration: 60 Minutes

Preventing Medical Device Recalls

CHARLES H. PAUL

Duration: 60 Minutes

Building a Compliant Documentation and Training System – 3 Hours Virtual Seminar

CHARLES H. PAUL

Duration: 3 Hour

New EU Medical Device Regulation – Everything That You Need To Know

CHARLES H. PAUL

Duration: 60 Minutes

US vs EU – Medical Devices Compliance and Regulatory Affairs

CHARLES H. PAUL

Duration: 60 Minutes

Risk Assessment for Medical Devices

CHARLES H. PAUL

Duration: 60 Minutes

Project Management for Non-Project Managers – 3 Hours Virtual Seminar

CHARLES H. PAUL

Duration: 3 Hour

Avoiding 483’s Throughout your Organization – Strategies, Risk and Mitigating Approaches

CHARLES H. PAUL

Duration: 60 Minutes

Line Clearance – Compliance Implications, Enforcement, and Best Practices

CHARLES H. PAUL

Duration: 60 Minutes

Good Manufacturing Practices - 3 Hours Virtual Seminar

CHARLES H. PAUL

Duration: 3 Hour

Human Error Prevention in Pharmaceutical Manufacturing

CHARLES H. PAUL

Duration: 60 Minutes

Writing Effective Standard Operating Procedure (SOPs) and Work Instructions (WIs)

CHARLES H. PAUL

Duration: 60 Minutes

GMPs for Medical Marijuana Production Operations

CHARLES H. PAUL

Duration: 60 Minutes

Complaint Handling Requirements – Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls, Life Cycle Process Activities

CHARLES H. PAUL

Duration: 60 Minutes

CE Marking in the EU – Latest Regulations

CHARLES H. PAUL

Duration: 60 Minutes

Good Clinical Practices Review of ICH E6 (R3) Latest Guidance

CHARLES H. PAUL

Duration: 60 Minutes

FDA vs EU Inspections - Differences And Similarities - How To Get Prepared

CHARLES H. PAUL

Duration: 90 Minutes

Project Management For Non-Project Managers - Getting The Project Off The Ground - Preliminary Project Planning

CHARLES H. PAUL

Duration: 2 Hour

Project Management for Non-Project Managers - Project Management in Drug Development

CHARLES H. PAUL

Duration: 90 Minutes

Project Management For Non-Project Managers Series - Project Management Process In Development Of In Vitro Diagnostics

CHARLES H. PAUL

Duration: 90 Minutes

Project Management For Non-Project Managers Series - Project Management As Applied To Clinical Trials

CHARLES H. PAUL

Duration: 90 Minutes

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

Drug Master Files (DMFS) - Understanding And Meeting Your Global Regulatory And Processing Responsibilities

CHARLES H. PAUL

Duration: 90 Minutes

GCP Risk Management And Risk-Based Monitoring

CHARLES H. PAUL

Duration: 90 Minutes

Annual GMP Master Class 2024

CHARLES H. PAUL

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

Good Clinical Practices (GCP) Audit And Inspection Readiness

CHARLES H. PAUL

Duration: 90 Minutes

Writing Investigations That Meet Regulatory Requirements

CHARLES H. PAUL

Duration: 90 Minutes

Business Continuity Planning For Contract Manufacturers In The Life Sciences

CHARLES H. PAUL

Duration: 90 Minutes

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

eCTD Submissions - Fundamentals and Process

CHARLES H. PAUL

Duration: 90 Minutes

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

How to Ace an FDA Meeting - Preparation and Conduct

CHARLES H. PAUL

Duration: 90 Minutes

GLP Data Integrity - Ensuring Accurate Reliable Results

CHARLES H. PAUL

Duration: 90 Minutes

Project Management for Non-Project Managers Series - Role of Project Management in Quality Planning Throughout the Medical Device Project Lifecycle

CHARLES H. PAUL

Duration: 2 Hour

ChatGPT and AI-Powered Project Management - Revolutionize your Projects Now

CHARLES H. PAUL

Duration: 60 Minutes

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

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