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 Research and Markets has announced the addition of the <a xmlns="http://www.w3.org/1999/xhtml" href="http://www.researchandmarkets.com/research/lsqz6c/latin_america" rel="nofollow" rel="nofollow">&#34;Latin 
 America: Regulatory Compliance Requirements for Life Science Products 
 BRAZIL Mexico, Argentina))): 2-day In-person Seminar&#34;</a> 
 conference to their offering.
 
 
 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.
 
 
 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.
 
 
 The current regulatory climate in Latin America is discussed in detail 
 and several examples will be provided to illustrate effective compliance 
 procedures and techniques. Common issues that have caused difficulties 
 for Life Sciences firms in the region are outlined. Course content will 
 explain how Latin America interacts with and utilizes ICH standards and 
 how they relate with other National Healthcare Authorities. 
 Additionally, participants will learn how personnel can best address the 
 conflicts, which arise and the best course for resolution.
 
 
 Who Should Attend:
 
 
 - Regulatory personnel whose responsibilities require knowledge of Latin 
 America&#39;s regulatory environment
 
 
 - Administrative staff responsible for ensuring compliance with 
 regulatory filings and overall regulatory compliance requirements will 
 also find this training highly relevant.
 
 
 - QA / QC Personnel
 
 
 - Global Supply Chain personnel
 
 
 - Clinical / Pharma &amp; Device personnel
 
 
 - Manufacturing personnel
 
 
 - Global Business Development personnel
 
 
 - Any sales or general management employee requiring an understanding of 
 how regulations and compliance issues impact the organization
 
 
 For more information about this conference visit <a xmlns="http://www.w3.org/1999/xhtml" href="http://www.researchandmarkets.com/research/lsqz6c/latin_america" rel="nofollow" rel="nofollow">http://www.researchandmarkets.com/research/lsqz6c/latin_america</a>
 
 
 
 
 
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Press Releases

Two Day Latin America Regulatory Compliance Requirements for Life Science Products Seminar: Focus on Brazil, Mexico, Argentina (San Diego, CA, United States - November 9-10, 2017) - Research and Markets 

BRAZIL

Two Day Latin America Regulatory Compliance Requirements for Life Science Products Seminar: Focus on Brazil, Mexico, Argentina (San Diego, CA, United States - November 9-10, 2017) - Research and Markets

TYO:6723


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Net income attributable to the Company increased by 34%.



The