Medical Devices 2012 - Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina)

This 4-hr Latin America Regulatory compliance requirements training/webinar 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.

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