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FDA Validation 2011 - Effective Facility Management, Operations and Maintenance in a Regulated Environment
Date2011-11-03
Deadline2011-11-03
VenuePalo Alto, USA - United States 
KeywordsFacility Management; FDA Regulated Companies; Maintenance Documents; FDA Guidelines; Facility Systems
Topics/Call fo Papers
In this 3-hr training on Facility Management you will learn how to develop thorough maintenance documents that are clear and confusion-free, and you will discover how to perform and document corrective work in a manner that eliminates ambiguity.
Why Should You Attend:
An ineffective facility management program can cost you thousands of dollars in lost production time and could lead to excessive exposure to regulatory audits.
Is your facility program comprehensive and proactive, or does your maintenance department spend more time in damage control mode?
Are your facility-related documents in need of a 'Quality' upgrade?
Do you secretly hope that regulatory auditors stay away from your critical utilities because of weaknesses in those areas?
Other CFPs
- Reduce COTS Software Validation using the risk-based approach
- Change Control Under the cGMPs and How the Regulations are Changing
- FDA's new enforcement initiative ? Strategic Software Validation Planning for Executives and Managers
- Risk Management in (FDA) Quality and Manufacturing Areas ? Understanding What the Regulators Expect and Working it to your Advantage
- GMP Requirements for Combination Products for the Medical Products Industry
Last modified: 2011-10-04 15:34:43