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” meansHow to manage the FDA’s 483 observations during and after an inspectionWhat the FDA considers importantHow to respond effectively to 483 observationsPlanning for other problemsLearn how to manage your regulatory profile with the FDAWho Will Benefit:Regulatory Affairs ProfessionalsIn-house Legal CounselSenior Managers for Manufacturing and Quality AssuranceFDA consultantsSenior Operations and Finance ExecutivesPublic Relations ProfessionalsSenior Executive ManagementMarketingPrice tags:LiveSingle Live : For One Participant$ 249Corporate Live : For Max. 10 Participants$ 899RecordingSingle REC : For One Participant - Unlimited Access for 6 Months$ 299For more information and enquiries contact us atCompliance Trainings5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada  Customer Support : #416-915-4458