Ace Bureau Seminar Series: Conformity Assessment Procedures for Medical Devices

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Submitted by superadmin on Wed, 03/06/2013 - 09:20

Date: 21st & 22nd March’2013
Exhibiting Booth: COEX (Convention & Exhibition Center) Hall A, Booth: A101
(World Trade Center 159 Samsung-dong, Gangnam-gu, Seoul 135-731, Korea)

Introduction

The seminar will provide attendees with an overview of the various conformity assessment procedures for Medical devices in the various markets of Europe, North America, Latin America, Middle East and Asia Pacific.

Such procedures are often pre-requisites for product entry into a foreign market and testing standards may vary from country to country. Non-compliance to such standards may prevent a product from entering a foreign country.

Hence, understanding these conformity assessment procedures around the world had far reaching benefits for International trade, helping companies reduce their technical barriers for market entry of their products.

Seminar overview

The highlight of the seminar is to bring you essential information that you may require in obtaining compliance for your products.

From this seminar, you will:

Learn about (Medical Device Directive) MDD 93/42/EEC conformity assessment procedures
Understand the requirement and procedures to plan and execute efficiently
Recognize various services that can help you comply with regulations
Obtain answers from experts to your compliance needs
Be able to plan an effective compliance road map for your business

Speaker's Profile

HeeSeon Eo
Sales Executive
ACE Bureau Singapore

George Azoury
CEO
RQSolutions Pty Ltd

Who should attend?

Manufacturers, Regulatory Affairs Professionals, Research and Development Professionals, Traders, Exporters, Marketing Managers, Quality Assurance Managers who are concerned about the future development of their business in international markets.

Cost of seminar:

Free

Seminar Outline

21st March’2013
Venue: COEX Conference Room 310

Time	Seminar Topic	Speaker
1400 - 1430 hrs	Registration
1430 - 1440 hrs	Introduction of Ace Bureau Company Profile	HeeSeon Eo
1440 - 1530 hrs	Certification for Medical and In-Vitro Device	HeeSeon Eo
End of Seminar

22nd March’2013
Venue: COEX Conference Room 314

Time	Seminar Topic	Speaker
1230 - 1300 hrs	Registration
1430 - 1440 hrs	CE marking for Medical and In-Vitro Device	HeeSeon Eo
1500 - 1515 hrs	Break Time
1515 - 1615 hrs	Worldwide approval for medical device Australia TGA Certification	HeeSeon Eo George Azoury
1615 - 1630 hrs	Break Time
1630 - 1700 hrs	New Proposal for EU Legislation on Medical and In-Vitro Device	HeeSeon Eo
End of Seminar

For more information

Please contact the respective staff for any clarifications:

Ms. HeeSeon Eo
Email: hseo@acebureau.org
Contact: +65-96415850
Fax: +65-62842918

Ms. Ellie Choi
Email: ellie@acebureau.org
Contact: +82-10-4433-7253