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One Day Seminar: Medical Device Regulations in Latin America (London, United Kingdom - February 11, 2019) - ResearchAndMarkets.com

November 30, 2018

DUBLIN--(BUSINESS WIRE)--Nov 30, 2018--The “Medical Device Regulations in Latin America” conference has been added to ResearchAndMarkets.com’s offering.

This new seminar will provide an essential overview of the key areas of requirements for approvals for medical devices in Latin America.

Focusing on the regulatory requirements and developments in individual countries, the course will include interactive discussion to allow you to exchange experiences with other colleagues.

Benefits of attending:

Understand medical device regulations in LATAM countries Learn the definition of Medical device and their classification Gain knowledge of the registration procedures Discuss recent developments in the region LATAM Opportunities to meet, network and share experience with other industry colleagues

Who Should attend?

This Seminar will be of particular interest to:

Anyone involved in the regulation for medical devices in LATAM Those who are new to working with medical devices in the region Anyone interested in an update on recent developments

Agenda:

Introduction to medical devices in the LATAM region

Competitive landscape overview and market opportunities Working with the national authorities How to co-ordinate regulatory operations in the region Mutual recognition and harmonisation Local importation requirements Which countries require permits/licences Working with local consultants and distributors

Brazil

Overview of medical device legislation in Brazil ANVISA regulatory approval process Overview of the IVD regulatory requirements in Brazil Medical Device Single Audit Programme (MDSAP)

Mexico

Understand the requirements of COFEPRIS regulation for medical devices Medical device classifications COFEPRIS registration routes Post-submission requirements Exploring strategies for bringing a medical device product to market in Mexico

Colombia and Peru

Legal overview of medical device regulations in these countries Medical device classifications Registration dossier requirements Renewal and variations Regulatory strategies to access these markets

Discussion sessions will take place throughout the day

For more information about this conference visit https://www.researchandmarkets.com/research/36ml54/one_day_seminar?w=4

View source version on businesswire.com:https://www.businesswire.com/news/home/20181130005295/en/

CONTACT: ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com

For E.S.T Office Hours Call 1-917-300-0470

For U.S./CAN Toll Free Call 1-800-526-8630

For GMT Office Hours Call +353-1-416-8900

Related Topics:Medical Devices

KEYWORD: UNITED KINGDOM BRAZIL EUROPE SOUTH AMERICA

INDUSTRY KEYWORD: HEALTH MEDICAL DEVICES

SOURCE: Research and Markets

Copyright Business Wire 2018.

PUB: 11/30/2018 10:16 AM/DISC: 11/30/2018 10:16 AM

http://www.businesswire.com/news/home/20181130005295/en

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