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

Website https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1550 | Edit Freely

Category Food, Drugs & Biologics

Deadline: March 24, 2015 | Date: March 24, 2015

Venue/Country: Mississauga, Canada

Updated: 2015-02-27 14:25:07 (GMT+9)

Call For Papers - CFP

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 : supportcompliancetrainings.com

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1550

Like Us On Facebook:

https://www.facebook.com/events/1619168248303672