Introduction
This 1 hour 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 hat 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
Ms HeeSeon Eo
Sales Executive
ACE Bureau Singapore
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
Exhibiting Booth
COEX (Convention & Exhibition Center)
Hall C, Booth number: C100
(World Trade Center 159 Samsung-dong, Gangnam-gu, Seoul 135-731, Korea)
Hall C, Booth number: C100
(World Trade Center 159 Samsung-dong, Gangnam-gu, Seoul 135-731, Korea)
Seminar Date and Time
- 16th February 2012 1 - 2pm
- 17th February 2012 1 - 2pm
- 17th February 2012 3 - 4pm
Please contact the respective staff for any clarifications:
Ms HeeSeon Eo
Email: hseo@acebureau.org
Contact: +82-11-9916-7470
Fax: +65-62842918
Seminar Outline
16th February 2012 (Conducted in Korean Language)
Venue: COEX Conference Room 317BC
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Time
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Seminar Topic
|
Speaker
|
|
1230 - 1300 hr
|
Registration
|
|
|
1300 - 1310 hr
|
Introduction of ACE Bureau Company profile
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
1310 - 1340 hr
|
Introduction to Europe MDD (Medical device directive)
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
1340 - 1400 hr
|
Introduction to Worldwide Medical device Certification
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
End of Seminar
|
||
17th February 2012 (Conducted in Korean Language)
Venue: COEX Conference Room 314
|
Time
|
Seminar Topic
|
Speaker
|
|
1230 - 1300 hr
|
Registration
|
|
|
1300 - 1310 hr
|
Introduction of ACE Bureau Company profile
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
1310 - 1340 hr
|
Introduction to Europe MDD (Medical device directive)
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
1340 - 1400 hr
|
Introduction to Worldwide Medical device Certification
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
End of Seminar
|
||
17th February 2012 (Conducted in English Language)
Venue: COEX Conference Room 314
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Time
|
Seminar Topic
|
Speaker
|
|
1430 - 1500 hr
|
Registration
|
|
|
1500 - 1510 hr
|
Introduction of ACE Bureau Company profile
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
1510 - 1540 hr
|
Introduction to Europe MDD (Medical device directive)
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
1640 - 1600 hr
|
Introduction to Worldwide Medical device Certification
|
HeeSeon Eo Sales Executive ACE Bureau Singapore
|
|
End of Seminar
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