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    "6-hr Virtual Seminar: Latin America ? Understanding Regulatory Compliance Requirements Across the Life Science Industry"

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    Website https://compliance2go.com/product/?pid=CP2014-295 | Want to Edit it Edit Freely

    Category online

    Deadline: July 22, 2014 | Date: July 22, 2014

    Venue/Country: Houston, U.S.A

    Updated: 2014-06-17 15:01:31 (GMT+9)

    Call For Papers - CFP

    DESCRIPTION

    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 asChile, 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.

    For any assistance contact us at supportatcompliance2go.com or call us at 877.782.4696 Or Visit us:-https://compliance2go.com/product/?pid=CP2014-295


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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