ComplianceOnline Webinar - Project Management for FDA-Regulated Companies(October 05, Tuesday 10:00 AM PDT | 01:00 PM EDT)

This FDA-Regulated webinar on Project Management will discuss and provide examples of most common project management tools and how to use it immediately to comply with FDA and EU MDD regulations.
Why Should You Attend:
The FDA expects companies to manage projects formally -- to include regulatory requirements, design and/or change control, with consideration of all applicable standards. The EU MDD and their notified bodies are no different.
This Project Management for FDA-Regulated Companies webinar will provide valuable guidance to regulated companies in development and implementation of Project Management Planning and Techniques for new product development, regulatory compliance audit responses, proof of "progress against plan", and other activities requiring a planned documented rationale. We will discuss one very simple approach using common Excel- or Word-type PC applications programs that can be used immediately. Three of the most common tools will be discussed. Regular use of a few simple but powerful tools will be showcased which will virtually eliminate "fire fighting" in a new project.
Areas Covered in the Seminar:

  • Why formal Project Management.
  • The three most common tools.
  • How to compile.
  • Gantt, CPM, PERT.
  • Simple construction techniques.
  • Work breakdown Structure, Milestones, Tasks.
  • Effectiveness -- Determining and Monitoring.
  • The "Example".

Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that need a repeatable methodology, and their in-house personnel trained in project management tools and techniques targeted specifically to the regulated medical products industries, under cGMP and MDD/CE-marking compliance. It will discuss and provide examples of the most common project management tools and provide a major example for immediate use. This applies to companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:

  • Senior management
  • Regulatory affairs
  • Quality Assurance / QAE
  • Production
  • R&D and Engineering

For More Information: