TMCnet News

Latin America: Regulatory Compliance Requirements for Life Science Products: Focus on Brazil, Mexico, Argentina - 2-day In-person Seminar (Burlingame, CA, United States - January 26-27, 2017) - Research and Markets
[January 03, 2017]

Latin America: Regulatory Compliance Requirements for Life Science Products: Focus on Brazil, Mexico, Argentina - 2-day In-person Seminar (Burlingame, CA, United States - January 26-27, 2017) - Research and Markets


Research and Markets has announced the addition of the "Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina): 2-day In-person Seminar" 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 Prducts 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.

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

For more information about this conference visit http://www.researchandmarkets.com/research/g9638q/latin_america


[ Back To TMCnet.com's Homepage ]