3-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry
This Latin America regulatory compliance requirements training will cover topics relating to pre-clinical and clinical requirements, as well as, addressing the structure of the regulatory agencies in Latin America. Why Should You 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 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 regulatory agencies. Additionally, participants will learn how personnel can best address the conflicts, which arise and the best course for resolution. Areas Covered in the Seminar: -Glossary of Terms. -Defining the Opportunity. -Country Facts: Argentina, Brazil, Mexico. -Latin America’s Regulatory Structure for the Life Science Product Industries -Mercosur – Southern Common Market. -Beginning Your Company Involvement in Latin America: Examples of Country Requirements. -Registration / Required Country Licenses. -Common Fees. Who Will Benefit: This course will be beneficial to: Regulatory personnel whose responsibilities require knowledge of Latin America’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 & 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 will also benefit Instructor Profile: Robert J. Russell, (Bob) is the President of RJR Consulting, Inc. RJR Consulting Inc. specializes in understanding global regulatory issues for the pharmaceutical industry. Bob has more than 25 years of experience working with FDA and the Commission on technical issues as they relate to policy development, regulation, clinical trial and the medical device development process. Prior to entering the consulting field, Mr. Russell was the Global Director of Regulatory Affairs for two Fortune 100 firms. These companies were major raw material suppliers to the pharmaceutical and medical device industry and one a joint-venture parent of a major pharmaceutical division. For Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702038?channel=limesfinder
