Regulatory Compliance Requirements for Life Science Products

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

Led by industry expert Robert J. Russell, ComplianceOnline’s popular seminar on regulatory compliance requirements for life science products comes to New Orleans, Philadelphia and San Diego in 2017. The two-day training program will address the structure of the regulatory agencies in Latin America and discuss local cultural nuances for working with the regulators.

This comprehensive course will cover topics ranging from pre-clinical and clinical requirements through product registration, amendments and renewals across life science products including pharmaceuticals, biologics, medical devices and combination products. The primary countries covered will include: Argentina, Brazil and Mexico. Other countries such as Chile, Costa Rica, Dominican Republic, Panama, Peru and Venezuela will also be discussed.

The 2016 ComplianceOnline Latin America regulatory compliance requirements seminar participation from various healthcare and pharma organizations, such as Pfizer Inc., Savant HWP Inc., Teva Pharmaceuticals, Ultragenyx Pharmaceutical Inc., Regeneron Pharmaceuticals, Inc. and others, have made the event an industry platform to reckon with.

This in-person training will assist regulatory affairs personnel, managers, QA/ QC teams, global supply chain personnel, manufacturing staff, and others within an organization.

Dates:

Thursday, May 18, 2017 (8.30 AM- 4.30 PM) and Friday, May 19, 2017 (8.30 AM- 4.30 PM)

Thursday, August 24, 2017 (8.30 AM- 4.30 PM) and Friday, August 25, 2017 (8.30 AM- 4.30 PM)

Thursday, November 9, 2017 (8.30 AM- 4.30 PM) and Friday, November 10, 2017 (8.30 AM- 4.30 PM)

Location 1: New Orleans, LA…

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