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2015 - Webinar On Managing the FDA form "483": Inspection Observations

Date2015-03-24

Deadline2015-03-24

VenueOnline, Canada Canada

KeywordsFDA form 483 Inspection; Fda inspection; 483 observations

Websitehttps://compliancetrainings.com/SiteEngi...

Topics/Call fo Papers

Description :
This webinar is a complete guide on how to manage the FDA's 483 observations during and after an inspection. How you respond can make or break you.
Areas Covered in the Session :
What the Form FDA “483” means
How to manage the FDA’s 483 observations during and after an inspection
What the FDA considers important
How to respond effectively to 483 observations
Planning for other problems
Learn how to manage your regulatory profile with the FDA
Who Will Benefit:
Regulatory Affairs Professionals
In-house Legal Counsel
Senior Managers for Manufacturing and Quality Assurance
FDA consultants
Senior Operations and Finance Executives
Public Relations Professionals
Senior Executive Management
Marketing
Price tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support-AT-compliancetrainings.com
For more information about this event please visit
https://compliancetrainings.com/SiteEngine/Product...
Like Us On Facebook:
https://www.facebook.com/events/1619168248303672

Last modified: 2015-02-26 22:53:52