US FDA 510(k): Due Diligence, Preparation, Submission and Clearance

US FDA 510(k): Due Diligence, Preparation, Submission and Clearance

 

About The Event

Product Format: Live Audio Conference
Presenter(s): Dr. David Lim, Ph.D., RAC, ASQ-CQA
Conference Date: Tue, Oct 08, 2013
Aired Time: 1 pm ET | 12 pm CT | 11 am MT | 10 am PT
Length: 60 Minutes
Price: $227

Get updated on demonstration of due diligence activity when contemplating a 510(k) submission, preparatory advice on a 510(k), its submission and clearance in accordance with FDA’s eCopy and RTA policy so that your skills and energy is effectively put to accelerate your 510(k) clearance, thereby saving your hard-earned money.

Join expert Dr. David Lim in this information packed 60-minute conference “US FDA 510(k): Due Diligence, Preparation, Submission and Clearance” on Tuesday, October 08, 2013, to understand the regulatory requirements for 510(k)s and Device classification and predicates

For more information:- US FDA 510(k): Due Diligence, Preparation, Submission and Clearance

Special Offer: Use code EVENT10% to get 10% discount.

For any queries feel free to contact Adam K at 1-866-458-2965 or e-mail Adam at customerservice@audioeducator.com.

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