FDA Validation 2011 - Effective Preparation for Audits and Inspections in a Regulated Environment - Webinar by ComplianceOnline
Date2011-11-17
Deadline2011-11-17
VenuePalo Alto, USA - United States
KeywordsProcess Validation; Biological Products; Process Development; QbD for Biological Products; QbD
Topics/Call fo Papers
This 3-hr FDA audit & Inspection training will focus on ideas that will help identify areas of improvement before the formal inspection occurs. Further, you will learn techniques that will enhance your effectiveness during the audit execution.
Why Should You Attend:
Many companies fail to prepare adequately for regulatory audits. Since inspectors can also appear unannounced, it is imperative to develop a compliance mindset so your facility is ready at all times for audits.
Are you prepared for a surprise inspection?
Do your employees know how to conduct themselves during an audit?
Are you confident in your ability to respond to difficult questions related to your manufacturing process?
Successful inspections require a well-thought out strategy and employees specifically trained on how to handle such inspections.
Other CFPs
- Process Validation for Biological Products ? Fitting PV into Process Development and QbD with New Regulations
- Effective Facility Management, Operations and Maintenance in a Regulated Environment
- 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
Last modified: 2011-10-04 15:50:24