ComplianceOnline Announces Seminar on Latin American Regulatory Requirements for Life Sciences Products

Top Quote ComplianceOnline, the leading GRC advisory network, and well known regulatory affairs expert Robert J. Russell will conduct a two day seminar on Latin American regulatory compliance requirements for life sciences products. End Quote
  • (1888PressRelease) January 05, 2013 - Palo Alto, CA, USA - ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced a seminar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina). The two day long seminar led by regulatory affairs expert Robert J. Russell will be held on February 11 and 12, 2013 in San Francisco, CA.

    For more information or to register for the seminar, please click here.

    Seminar instructor Robert J. Russell is the president of RJR consulting Inc., which specializes in global regulatory issues for the pharmaceutical industry. He has more than 25 years of working experience with FDA and the Commission on technical issues as they relate to policy development, regulation, clinical trial and the medical device development process. He was also the global director of regulatory affairs for two Fortune 100 firms.

    During the two day interactive seminar, Mr. Russell will focus on the overall regulatory compliance requirements and procedures for pharmaceuticals, medical devices, biologics and combination products in Latin America. The primary countries covered are Argentina, Brazil and Mexico. Other countries which will be discussed are Chile, Costa Rica, Dominican Republic, Panama, Peru and Venezuela. The course will cover topics related to pre-clinical and clinical requirements and the current regulatory climate in Latin America. Mr. Russell will explain the common issues that have caused difficulties for life sciences firms in Latin America and will provide the attendees an understanding on how to best address the conflicts, which arise and the best course for resolution.

    The seminar will be valuable for any regulatory personnel whose responsibilities require knowledge of Latin America's regulatory environment, administrative staff, QA/ QC personnel, global supply chain personnel, manufacturing personnel, global business development personnel and any clinical/pharma and device personnel.

    Date: Monday, February 11 and Tuesday, February 12, 2013, 8AM- 4 PM PST
    Venue & Location: Grand Hyatt San Francisco
    345 Stockton Street,
    San Francisco, CA 94108

    Registration Cost: $1,499.00 per registration
    Early bird discounts: For discounts on early registrations, please click here .
    Register by phone: Please call our customer service specialists at +1-650-620-3937 or email to customercare ( @ ) complianceonline dot com

    For more information on ComplianceOnline or to browse through our trainings, please visit our website.

    About ComplianceOnline
    ComplianceOnline is a leading provider of regulatory/compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 20,000 professionals from 3,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at

    For more information please contact:
    A Reuben Bernard
    Manager of Program Marketing
    2600 E Bayshore Rd
    Palo Alto CA USA 94303
    650-620-3937 phone
    650-963-2530 fax
    reuben ( @ ) complianceonline dot com

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