Thursday, April 10, 2014
1:30 pm - 3:00 pm EDT
12:30 pm - 2:00 pm CDT
11:30 am - 1:00 pm MDT
10:30 am - 12:00 pm PDT
6:30 pm - 8:00 pm BST
CDRH has recently overhauled its Office of Compliance — what exactly has changed and what hasn’t? What does your team need to know going forward in order to deal with the Office of Compliance? What does the OC expect from you?
These are just a few of the important questions you need to ask. There is only so much you can learn from the diagrams and organizational charts provided by the FDA.
Mark your calendar for Thursday, April 10, when we’ll rebroadcast Steve Niedelman’s and Steve Silverman’s immensely popular webinar on compliance reorganization.
Here’s what our satisfied registrants had to say on what they liked about this webinar:
Register now for this exclusive rebroadcast question-and-answer webinar with FDA veteran Steve Niedelman, lead quality systems and compliance consultant to the FDA & Life Sciences practice team at King & Spalding, as he speaks with Steve Silverman, Director of CDRH’s Office of Compliance, to help you understand all the changes.
With the recent reorganization, the OC will sharpen its focus on international inspections and audits on labeling.
CDRH has also replaced the OC’s former four–division structure with five divisions, with each division containing a number of sub-branches. The divisions are as follows:
There’s just one low registration fee per site regardless of how many participate. Generous multi-site discounts are available, too. Simply call (888) 838-5578 in the US or +1 (703) 538-7600 globally. Please note; this webinar has been previously recorded and no questions will be taken during the presentation.