Date :
Place : United States, Aurora
Website :https://goo.gl/2HTZ1R
Contact Person:Training Doyens
Description:
Know about the new changes introduced by the FDA in its import program for managing issues along with the new procedures introduced to make the whole process better.Deadline for abstracts/proposals : 26th March 2018
Organized By :Training Doyens
Keynote Speakers : David R. Dills, Global Regulatory Affairs & Compliance Consultant, Interim President, currently provides global regulatory affairs, compliance and quality consultative services for early-stage and established Class I/II/III medical device, including combination products, In Vitro Diagnostics, nutraceuticals/supplements, cosmetics and biopharmaceutical manufacturers in multiple medical specialties and therapeutic areas on the global landscape, and has an accomplished record with more than 26
Conference Highlights :OVERVIEW FDA and U.S. Customs and Border Protection are using new import requirements.The FDA’s import software screening program (PREDICT) and the U.S. Custom’s ACE software program require more information from the foreign source(s). FDA’s product codes and U.S. Harmonized Tariff Schedule (HTS) link the requirements. Take away is that the software coding information must be correct. Otherwise, you face costly delays and possibly a refusal of the entry. In addition, information on the en
Venue :26468 E Walker Dr, Aurora, Colorado 80016, USA
Check the event website for more details.