Return-Path: Delivered-To: charley@transocean.com Received: from vps.transocean.com by vps.transocean.com with LMTP id kGc0GnvKzFpsagAAInt2oQ for ; Tue, 10 Apr 2018 07:30:19 -0700 Return-path: Envelope-to: charley@transocean.com Delivery-date: Tue, 10 Apr 2018 07:30:19 -0700 Received: from mta034b.pmx1.epsl1.com ([142.54.244.34]:51141) by vps.transocean.com with esmtp (Exim 4.89_1) (envelope-from ) id 1f5uHi-0007Ot-CZ for charley@transocean.com; Tue, 10 Apr 2018 07:30:19 -0700 DKIM-Signature: v=1; a=rsa-sha256; c=simple/simple; d=info.complianceonline.com; s=ep1; t=1523370571; bh=lhgTy5XFoZiMY7UKszCsOO7HEWfoIkK5KyOTikGYaNs=; h=MIME-Version:Subject:From:To:Date:Content-Type; b=GPloa/PlVYhKn5zt4seiAh1BWFscbC9vf6VnqJvKQtvVGhfecq73b5I6vO8GdzBFm +sqcWf5PhNoBWrj2yNUgV9wTlwgiUrOVrfIudI0kVcBHDfXHWXHXfYQ3AbAM5rsAUU AE3BOCy+52MOmTmEMDP3HtQSm8j3BxH7FBAmbkw8= Received: from [10.233.19.41] ([10.233.19.41:35462]) by pc1udsmtn1n12 (envelope-from ) (ecelerity 3.6.9.48312 r(Core:3.6.9.0)) with ECSTREAM id B6/CD-43926-B4ACCCA5; Tue, 10 Apr 2018 14:29:31 +0000 List-Unsubscribe: Message-ID: MIME-Version: 1.0 Reply-To: "training@info.complianceonline.com" Subject: FDA's New Import Program for 2018 - Strict Precision | Seminar by Ex-FDA Official From: compliance seminar To: charley@transocean.com Date: Tue, 10 Apr 2018 14:29:31 +0000 Content-Type: multipart/alternative; boundary="-=Part.3a2e50c.f2db74fe3cb5cbf0.162aff63523.cb35b27f8c3b42d0=-" X-Spam-Status: No, score=1.4 X-Spam-Score: 14 X-Spam-Bar: + X-Ham-Report: Spam detection software, running on the system "vps.transocean.com", has NOT identified this incoming email as spam. The original message has been attached to this so you can view it or label similar future email. If you have any questions, see root\@localhost for details. Content preview: ComplianceOnline ComplianceOnline The Largest GRC Advisory Network +1-888-717-2436 FDA's New Import Program for 2018 - Strict Precision 2-Day In-Person Seminar by Ex-FDA Official DoubleTree by Hilton San Francisco Airport, CA -- June 28-29 • View Agenda Speaker: Casper E. Uldriks, Former Associate Center Director of FDA's CDRH The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier. The FDA and U.S. Customs and Border Protection (CBP) are relying more and more on computer programs to expedite the import process. When and how you use these programs can make a big difference in the net profit derived from even a single shipment. The new Voluntary Qualified Importer Program (VQIP) is one such example. Another example is CBP's and FDA's implementation of the Automated Commercial Environment (ACE) program became mandatory for importers in 2016. If you fail to correctly use new import procedures and programs, you will be operating under an expensive disadvantage. Register Now Learning Objectives: FDA's new cost-saving import programs Understand how U.S. Customs and FDA legal requirements intersect Know how to manage foreign suppliers Understand FDA's internal procedures Learn how to mitigate and resolve import detentions Learn how to avoid common problems Develop practical ways to improve your import and export business You will be able to answer the following questions with this course without saying, “I don't know?” What are the FDA's import legal requirements and policy? How do you deal with the FDA and the U.S. Customs and Border Patrol procedures? What happens when your product is detained? What happens if a foreign manufacturer is in trouble with the FDA? How do you inter-act with the FDA to work out problems? Why are import and export rules different or does it even matter? Speaker Profile: [...] Content analysis details: (1.4 points, 3.0 required) pts rule name description ---- ---------------------- -------------------------------------------------- 0.0 URIBL_BLOCKED ADMINISTRATOR NOTICE: The query to URIBL was blocked. See http://wiki.apache.org/spamassassin/DnsBlocklists#dnsbl-block for more information. [URIs: complianceonline.com] -0.0 SPF_PASS SPF: sender matches SPF record 0.7 MIME_HTML_ONLY BODY: Message only has text/html MIME parts 0.0 HTML_MESSAGE BODY: HTML included in message -0.0 BAYES_40 BODY: Bayes spam probability is 20 to 40% [score: 0.2467] 0.8 MPART_ALT_DIFF BODY: HTML and text parts are different -0.1 DKIM_VALID_AU Message has a valid DKIM or DK signature from author's domain 0.1 DKIM_SIGNED Message has a DKIM or DK signature, not necessarily valid -0.1 DKIM_VALID Message has at least one valid DKIM or DK signature 0.0 MIME_HTML_ONLY_MULTI Multipart message only has text/html MIME parts X-Spam-Flag: NO ---=Part.3a2e50c.f2db74fe3cb5cbf0.162aff63523.cb35b27f8c3b42d0=- Content-Transfer-Encoding: quoted-printable Content-Type: text/html; charset=UTF-8 ComplianceOnline
Comp= lianceOnline
The Largest GRC Ad= visory Network 		+1-888-717-24= 36
FDA's New Imp= ort Program for 2018 - Strict Precision
2-Day In-Person Seminar by Ex-FDA O= fficial
DoubleTree by H= ilton San Francisco Airport, CA -- June 28-29 =E2=80=A2 View Agenda<= /td>
<= strong>Speaker: Casper E=2E Uldriks, Former Assoc= iate Center Director of FDA's CDRH
The FDA continues to change its import program to better manage n= ew problems and to use new procedures to make the whole process easier=2E T= he FDA and U=2ES=2E Customs and Border Protection (CBP) are relying more an= d more on computer programs to expedite the import process=2E When and how = you use these programs can make a big difference in the net profit derived = from even a single shipment=2E The new Voluntary Qualified Importer Program= (VQIP) is one such example=2E Another example is CBP's and FDA's implement= ation of the Automated Commercial Environment (ACE) program became mandator= y for importers in 2016=2E If you fail to correctly use new import procedur= es and programs, you will be operating under an expensive disadvantage=2E <= br />
Register Now

Learning Objectives:
  • FDA's new cost-saving import programs
  • Understand how U=2ES=2E Customs and FDA legal requirements intersect
  • Know how to manage foreign suppliers
  • Understand FDA's internal procedures
  • Learn how to mitigate and resolve import detentions
  • Learn how to avoid common problems
  • Develop practical ways to improve your import and export business
  • You will be able to answer the following questions with this course wi= thout saying, =E2=80=9CI don't know?=E2=80=9D
  • What are the FDA's import legal requirements and policy?
  • How do you deal with the FDA and the U=2ES=2E Customs and Border Patro= l procedures?
  • What happens when your product is detained?
  • What happens if a foreign manufacturer is in trouble with the FDA?
  • How do you inter-act with the FDA to work out problems?
  • Why are import and export rules different or does it even matter?
Speaker Profile:

Seminar Instructor Casper Uldriks is an "Ex-FDA Official" who has spent 32 years in = FDA and his engagements focus on advertising and promotion, recalls, correc= tions and removals and enforcement=2E He currently trains FDA personnel and= counsels clients on wide range of topics, including: FDA inspections; impo= rt operations; advertising and promotion; corrective and preventive actions= ; medical device reporting and corporate reorganization to improve conforma= nce to the FDA's requirements=2E
View Details
4th Annual Medical Device Summit 2018 | San Franci= sco, CA | June 7-8, 2018
=C2=A9 Copyright 2018 | 2479 East Bayshore Road, Suite 200 = Palo Alto, CA 94303, USA | +1-888-717-2436
This message was sent to charley@transocean=2Ecom | Unsubscribe=2E
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