Food - Current and Future Safety Regulations - 2017

  • Check with publisher
  • Published date: May 15, 2017
    • Fremont, California, United States

Importers of food products intended for introduction and consumption in

the United States through international commerce are responsible for

ensuring that the products are safe, sanitary, wholesome, and labeled

according to U.S. requirements.

Areas Covered in the Session:
Understand "Prior Notice" requirements
Foreign Supplier Verification Program (FSVP)
Prepare for the Foreign Facility Inspection Program
Learn what is in the “Investigations Operation Manual (IOM)
What can happen to your product when seized
Learn what other countries require for food import

Who Will Benefit:
Food buyers
Foreign food producers and exporters
International food carriers
Import and export logistics personnel
Foreign facility food safety specialists
Food import companies

Speaker Profile:
Dr. John Ryan's quality system career has spanned the manufacturing, food,

transportation and Internet industries over the past 30 years. He has

worked and lived extensively throughout Asia and the U.S. at the corporate

and facility levels for large and small companies as a turn-around specialist.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407

Full Details & Registration Link:

0 votes

Useful information

  • Avoid scams by acting locally or paying with PayPal
  • Never pay with Western Union, Moneygram or other anonymous payment services
  • Don't buy or sell outside of your country. Don't accept cashier cheques from outside your country
  • This site is never involved in any transaction, and does not handle payments, shipping, guarantee transactions, provide escrow services, or offer "buyer protection" or "seller certification"

Related listings

  • Lead Clinical Research Associate Job - Princeton, NJ

    Lead Clinical Research Associate Job - Princeton, NJ

    Clinical Princeton (New Jersey) December 14, 2017 Check with publisher

    Purpose Responsible for the performance of assigned sites within assigned trials in accordance with Good Clinical Practice (GCP), International Council of Harmonisation (ICH) guidelines, federal regulations and Standard Operating Procedure (SOPs). Re...