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Medical Device 2012 - Project Management To Meet CGMP Requirements
Date2012-03-20
Deadline2012-03-20
VenuePalo Alto, USA - United States 
KeywordsFDA regulatory compliance training EU MDD regulations compliance; Project management compliance; FDA project management regulations; FDA compliance training
Topics/Call fo Papers
This Project Management training for FDA Regulated Companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage. It will focus on proven tools and techniques for successful development and implementation of project management planning
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.
Other CFPs
- Understanding Design Controls for Medical Devices
- Advanced Methods of Root Causes Analysis for ISO 14971 Risk Reduction
- Complaint Handling in Compliance with FDA and ISO Regulations
- Medical Device Regulations and Law in the US, EU and Canada
- Understanding Disinfection and Cleanroom Cleaning in a FDA Regulated Environment
Last modified: 2012-01-23 15:29:14