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

    View: 231

    Website http://bit.ly/1viGxro | Want to Edit it Edit Freely

    Category FDA Compliance;

    Deadline: January 26, 2017 | Date: January 26, 2017-January 27, 2017

    Venue/Country: Burlingame, U.S.A

    Updated: 2016-12-09 21:02:27 (GMT+9)

    Call For Papers - CFP

    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.

    Why You Should 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 the wide array of licensed products.

    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

    Note:

    Use coupon code NB5SQH8N and get 10% off on registration.

    For Registration:

    http://www.complianceonline.com/latin-america-regulatory-compliance-requirements-for-life-science-products-focus-brazil-mexico-argentina-seminar-training-80016SEM-prdsm?channel=ourglocal


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.