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


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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.

The current regulatory climate in Latin America is discussed in detail and several examples will be provided to illustrate effective compliance procedures and techniques. Common issues that have caused difficulties for Life Sciences firms in the region are outlined. Course content will explain how Latin America interacts with and utilizes ICH standards and how they relate with other National Healthcare Authorities. Additionally, participants will learn how personnel can best address the conflicts, which arise and the best course for resolution.

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
Day 01(8:30 AM - 4:30 PM)
  • 8:30 – 9:00 AM: Registration
  • 9:00 AM: Session Start Time
    • LA Overview
    • LA markets
    • Harmonization efforts
    • Understanding the Regulatory Process
    • Regulatory Overview (gov't offices, organization, contact info)
      • Brazil - ANVISA
      • Mexico – COFEPRIS
      • Argentina – ANMAT
    • Country Establishment
    • Clinical Trials
      • Clinical Trial Start-up
      • Clinical Trial Application
      • IND's
      • Reporting
      • GCP
    • Scientific advice
    • Stability studies
    • Pharmaceuticals
      • Marketing Authorizations/Registrations
      • Registration requirements
      • Registration documentation/CTD
      • Summary of Product Characteristics
      • Package insert
      • Labeling
      • Pharmacovigilance/Post-marketing
      • Amendments/Variations/Changes/Renewals
      • Fees
    • Submission Process
    • Paper filings
    • Electronic filings
Day 02(8:30 AM - 4:30 PM)

    • Generics & Bioequivalence
    • Biologics
    • Compassionate use
    • Orphan drugs
    • Medical Devices
      • Device Classification
      • Testing Standards
      • Registrations
      • Amendments/Variations/Renewals
      • Cost build-up model
      • Fees
      • Post-marketing
    • Combination products
    • Patents/Copyrights/Trademarks
    • Import/Export procedures
    • Tax exemptions
    • Advertising/Promotion
    • Comparing & Contrasting LA and US
    • Challenges in Latin America
    • Influencing the Regulatory Process
    • Conclusions & summary
Seminar (Price/Register)
Seminar Fee Includes:
Lunch
AM-PM Tea/Coffee
Seminar Material
Attendance Certificate
$100 Gift Cert for next seminar

Other Registration Option
  1. Download the Order Form
  2. Fill this form with attendee details & payment details
  3. Fax your PO to 1-888-883-7697 or,
  4. Email it to cs@compliance.world

Payment Mode

By Check -

Pay your check issued from the payee to "Redstone Learning Inc." (Our Parent Company) and mail the check to –
Compliance.world (Redstone Learning Inc.)
1180 Avenue of the Americas,
8th Floor, New York,
NY 10036

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Speaker: Robert J. Russell,

Robert J. Russell, (Bob) is the President of RJR Consulting, Inc. RJR Consulting Inc. specializes in understanding global regulatory issues for the pharmaceutical industry. Bob has more than 25 years of experience working with FDA and the Commission on technical issues as they relate to policy development, regulation, clinical trial and the medical device development process. Prior to entering the consulting field, Mr. Russell was the Global Director of Regulatory Affairs for two Fortune 100 firms. These companies were major raw material suppliers to the pharmaceutical and medical device industry and one a joint-venture parent of a major pharmaceutical division.


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