Importing and Exporting Covid-19 Products
October 15, 2020 - CA USCompliance4All
support@compliance4All.com
Phone:8004479407
Overview: The outbreak of coronavirus disease (COVID-19), first in the People's Republic of China (PRC or China), and now globally, including in the United States, is drawing attention to the ways in which the United States and other economies depend on critical manufacturing and global value chains that rely on production based in in the PRC and other countries. Congress is particularly concerned about these dependencies and has passed legislation to better understand and address them. An area of particular concern to Congress in the current environment is U.S. shortages of medical supplies -including personal protective equipment (PPE) and pharmaceuticals - as the United States steps up efforts to contain COVID-19 with limited domestic stockpiles and insufficient U.S. industrial capacity. PPE, antibiotics, and active pharmaceutical ingredients have led to shortages of critical medical supplies in the United States. Importers and exporters of Covid-19 products need to know how to handle these products, avoid problems and penalties, while helping those who desperately need such products. Why you should Attend: This webinar is an important step in helping importers and exporters understand and appreciate the standards established by CBP the largest U.S. law enforcement agency - the FDA and FEMA with regard to PPE - like masks/respirators, face shields, gowns, and other items considered to be medical devices. U.S. importers and exporters must exercise extreme care when importing goods into and exporting PPE products from the United States. The failure to understand or appreciate the complex nature of CBP, FDA, FEMA, and other agency regulations can and do result in detentions and seizures, significant fines and penalties, the loss of customers, and lots of aggravation. U.S. agencies are now engaged in enforcement actions that can ruin actual and prospective importers and exporters of PPE. Learn what PPE is equipment intended for medical use by healthcare professionals in hospitals and medical facilities; and what equipment intended for general purpose or industrial use (that is, not intended to be distributed or marketed for medical use). Discover how to banish fear, uncertainty and doubt with regard to the import or export of Covid-19 products. You need to know what you are doing. Areas Covered in the Session: FDA-regulated products for medical use FDA classification of medical products CBP HTSUS classification of PPE FDA regulatory requirements for imported PPE CBP regulatory requirements for imported PPE National Institute for Occupational Safety and Health (NIOSH) concerns FDA's Emergency Use Authorization (EUA) authority Non-FDA regulated products for general purpose or industrial use China and other country export restrictions Defense Production Act CBP, FEMA and exporting PPE Government import and export seizures of PPE Penalties How to stay compliant Who Will Benefit: Importers Exporters Business owners Manufacturers Accountants Medical Doctors Nurses Other Healthcare Workers Lawyers Anyone involved in the import or export of Covid-19 products Speaker Profile Martin K.Behr, III is a customs and international trade lawyer admitted to practice in New Jersey, New York and Pennsylvania, and before the U.S. District Court for the District of New Jersey and the U.S. Court of International Trade. Martin received a Bachelor of Arts degree from Rutgers University - Newark, Phi Beta Kappa, with high honors; a Master of Public Administration degree from Fairleigh Dickinson University; and a law degree from Rutgers School of Law - Newark. Martin is a distinguished graduate of both the U.S. Law Enforcement Training Center and the U.S. Customs Service Academy. He is also a licensed U.S. Customs Broker (No. 20643), one who worked in the industry for several years.