ComplianceOnline

Medical Device Registration - Brazil and Argentina

Instructor: Eliana Silva de Moraes
Product ID: 705658
  • Duration: 90 Min

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Apr-2018

Training CD / USB Drive

$399.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

Learn how to design regulatory strategy for your medical device to expand your business in Brazil & Argentina. Get insight in to regulatory policy and implication for medical device and the key issues in medical device laws of Brazil and Argentina.

Why Should You Attend:

When considering expanding or relocating to the Brazil and Argentina, companies typically focus on business decisions and often neglect to the design a specific regulatory strategy, even though regulatory issues are an important in an effective business plan. For this reason, the first thing a company that intends to launch a product in the region has to realize is the regulatory affairs landscape.

Learn from the expert who played an active role in setting up Brazil’s Public Health Regulator (ANVISA), about the recent news/update about medical device registration system in Brazil and Argentina. You will get a comprehensive insight in the regulatory policy and implication for medical device approval in Brazil and Argentina. An opportunity to analyze and discuss key issues in medical device law. Many theoretic cases with exercises examples will be presented in this webinar.

Areas Covered in the Webinar:

  • Overview of challenges and opportunities in the development of business in Brazil and Argentina
  • How to develop a very good and effective regulatory affairs strategy to have success in the region
    • Medical Device Approval in Brazil and Argentina
    • Launching a medical device in Brazil and Argentina
    • Submission, renewals and variations of the marketing authorization
  • Understanding how to save time and money with your RA strategy in the region
    • Harmonization RA process
    • Regulatory Affairs strategies
    • Polices to meet the applicable regulations
  • Comprehensive overview of the necessary steps of Regulatory Affairs procedures in Brazil and Argentina
    • Advertisement, Techno vigilance; Documentation Requirements
    • Mergers & acquisitions, large and smaller transactions
  • The important legal issues to pay attention in order to get your product approval
    • Legal department; multiple departments of relevant regulatory issues
    • Registration submission, renewals and variations of the marketing authorization
  • Best practices of preparation of documents and submission of application to the Agencies

Who Will Benefit:

  • Head of Regulatory Department
  • Individuals
  • Supply chain
  • Heads of Purchase Department
  • Projects Head
  • Project Manager
  • Head of Regulatory Department
  • Regulatory Consultant
  • Head of Quality Control
  • Technical Responsible
  • Head of Legal Dept
  • Project Marketing
  • Head of IT Department
Instructor Profile:
Eliana Silva de Moraes

Eliana Silva de Moraes
President, Brazilian Regulatory Affairs

Eliana Silva de Moraes is a Lawyer, specializing in Public Health Law (1992), graduated in Public Health Law, by Public Health School - University of Sao Paulo (1995); master degree (II) in Biomedical Law University of Coimbra, Portugal (2005), Ph.D. in European Regulatory on Public Health Law by Paris VIII University. 26 years’ experience in Pharmaceutical law, Food law, Cosmetic law, Medical Device and Equipment law, Pharmaceutical and Veterinary product for Brazil and Latin America countries, for administrative, litigation and facilitator process.

Played an active role in setting up Brazil’s Public Health Regulator (ANVISA), organizing the agenda of its first President in USA in order to explore the US System established through the Food and Drug Administration (FDA) in December 1998 as well as in the global harmonization process.

Follow us :
Managing Your Complaints and Obstacles in Post-Market Requirements
Vendor and Supplier Qualification Program for FDA Regulated Industries

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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