Return-Path: Delivered-To: charley@transocean.com Received: from vps.transocean.com by vps.transocean.com with LMTP id aJpnHbdrz1q5cQAAInt2oQ for ; Thu, 12 Apr 2018 07:22:47 -0700 Return-path: Envelope-to: charley@transocean.com Delivery-date: Thu, 12 Apr 2018 07:22:47 -0700 Received: from mta.email.complianceonline.com ([198.31.63.221]:16454) by vps.transocean.com with esmtp (Exim 4.89_1) (envelope-from ) id 1f6d7Y-0007Zf-Gu for charley@transocean.com; Thu, 12 Apr 2018 07:22:47 -0700 DKIM-Signature: v=1; a=rsa-sha1; d=email.complianceonline.com; s=ei0; c=simple/simple; q=dns/txt; i=@email.complianceonline.com; t=1523542876; h=From:Subject:Date:To:MIME-Version:Content-Type; bh=mo478bvPIxmnC/PlANeOqFE9emE=; b=slrq2h8WWuc5S2YNbsYP86Nui/6tsYtSypz1AKEi3vR+rAAdGBAp/DcvqYxBKxzB 8c5Zu4HS33kcNk1KGeD0W/0rMKOUTGz79jnw7FCJdda+G6TM1VV8bV5Epj+RhAwX bqTDFeHFqCDz1UHJFACWhiByZYW7BhMeexVkrb5AawI=; Received: from [10.21.250.232] ([10.21.250.232:4616] helo=CORE18PUMPER2) by pc1udsmta1n24 (envelope-from ) (ecelerity 2.2.2.45 r(34222M)) with ESMTP id E7/26-01546-C5B6FCA5; Thu, 12 Apr 2018 10:21:16 -0400 Date: Thu, 12 Apr 2018 23:21:16 +0900 (JST) Message-Id: X-DMHA-ID-Packet: Z4gvK5o622gzTBxIWzQ7JzhVn6wQZ9VFYlyNwgUtkUt4De_O9mstCVgBBcYEXG9As2khkdGXmNw= From: "compliance seminar" Reply-To: "Editor complianceonline" To: charley@transocean.com Subject: Latin America Regulatory Requirements for Life Science Products | New Orleans, LA MIME-Version: 1.0 Content-Type: text/html; charset="us-ascii" Content-Transfer-Encoding: 7bit X-Spam-Status: No, score=0.6 X-Spam-Score: 6 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 Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) Courtyard New Orleans French Quarter, LA | May 31-June 1, 2018 • View Agenda Speaker: Robert J. Russell, President of RJR Consulting, Inc. This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and renewals across Pharmaceuticals, Biologics, Medical Devices and Combination Products. The Course will address the structure of the regulatory agencies in Latin America and discuss local cultural nuances to help you be successful in working with the regulators. Register Now Why You Should Attend: [...] Content analysis details: (0.6 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 0.0 HTML_MESSAGE BODY: HTML included in message 0.7 MIME_HTML_ONLY BODY: Message only has text/html MIME parts -0.0 BAYES_20 BODY: Bayes spam probability is 5 to 20% [score: 0.1708] -0.1 DKIM_VALID Message has at least one valid DKIM or DK signature -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 X-Spam-Flag: NO ComplianceOnline
ComplianceOnline
The Largest GRC Advisory Network 		+1-888-717-2436
Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)
Courtyard New Orleans French Quarter, LA | May 31-June 1, 2018 • View Agenda
Speaker: Robert J. Russell, President of RJR Consulting, Inc.
This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and renewals across Pharmaceuticals, Biologics, Medical Devices and Combination Products. The Course will address the structure of the regulatory agencies in Latin America and discuss local cultural nuances to help you be successful in working with the regulators.
Register Now

Why You Should Attend:

This course specifically focuses on the overall regulatory compliance requirements and procedures for Pharmaceuticals, Medical Devices, Biologics and Combination Products in Latin America. The primary countries covered will include: Argentina, Brazil and Mexico. Other countries such as Chile, Costa Rica, Dominican Republic, Panama, Peru and Venezuela will be discussed. The course will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Latin America. Content will include descriptions of the methods by which regulators in the corresponding agencies process filings and registrations and what is expected in the authorization and dossier maintenance of the wide array of licensed products.

Speakers Profile:

Robert J. Russell, (Bob) is the President of RJR Consulting, Inc., a Global Regulatory Consulting company, specializing in understanding regulatory issues for the pharmaceutical, medical device and combination products industry. Bob has more than 30 years of experience working with FDA, EMA, Healthcare Authorities and Agencies across Latin America, Middle East and Asia / Pacific supporting clients projects in these regions. Licensing, registrations, GMP, DMFs and borderline products are core competencies of the Course Director.
View Details
4th Annual Medical Device Summit 2018 | San Francisco, CA | June 7-8, 2018
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