ONLINE & IN TOUCH!
JUNE 3 - NOVEMBER 11, 2021
8 GREAT ONLINE EVENTS!
Insights & Expertise
LIVE WEBINARS + Q&A SESSIONS
Global Medical Device Focus 2021
FROM CONCEPT TO MARKET ACCESS. FROM SOUTH AMERICA TO ASIA.
DISCOVER THE ESSENTIALS THAT MAKE MEDICAL DEVICE SUCCESS A REALITY!
Come join the medical device industry's leading experts and authorities in global clinical research and regulatory affairs for an exciting program of discovery and exchange. With a diverse array of topics and discussions to choose from, there's something for everyone at the Global Medical Device Focus 2021. This great opportunity will help participants learn what it takes to successfully plan, implement, and obtain successful medical device registrations throughout various countries and regions around the world.
Business & Regulatory
Discover how you can optimize revenue by planning early for your medical device global market access.
Clinical Evaluation
How to conduct global clinical investigations? Learn what data is needed to access world markets including China.
Live Q&A sessions
You've got the questions; we have the answers!
Program & Registration
Global Medical Device Focus 2021
The world's top medical device experts at your finger tips.
Global Medical Device Focus 2021 brings you the medical device industry's leading experts and authorities in clinical research and regulatory affairs from around the world to discover what it takes to successfully plan, implement and obtain medical device registration throughout Asia Pacific, Middle East, and South American markets.
Be sure to check out these 8 great events:
THURSDAY, JUNE 3 11:00am-1:30pm CEST
INDONESIA
- Overview of Current Medical Device Regulations in Indonesia
Maura Linda Sitanggang – former Director General of Pharmacy and Medical Device Ministry of Health of Republic of Indonesia reporting directly to the Minister of Health - Conducting Medical Device Clinical Investigations in Indonesia
Ivon Septriyana, Clinical Project Manager S-E Asia, MD-Clinicals - Practical Approach to Getting Devices to the Indonesian Market
Ella Siti Alawiyah, Gakeslab - Q&A session
Access provided by WMDO.ORG
THURSDAY, JUNE 10 11:00am-1:30pm CEST
SINGAPORE & MALAYSIA
- Singapore Implementation of UDI
Andrew Ho, DHReg-Sys - Malaysia Update on Medical Device Regulation Implementation
Anis Adila, DHReg-Sys - Current Experience with Compliance to Medical Device Regulations in Malaysia
Syazwani Binti Zakariya, CARE Certification International Sdn Bhd - Conducting Clinical Investigations in Singapore vs. Malaysia
Ivon Septriyana, Clinical Project Manager S-E Asia, MD-Clinicals - Q&A session
Access provided by WMDO.ORG
THURSDAY, JUNE 17 11:00am-1:30pm CEST
THAILAND & VIETNAM
- Latest Updates for Medical Device Regulations in Thailand
Raenu Chaichanan - Updates of the Recent Medical Device Regulation in Vietnam
Chi Thanh Nguyen, Vietnam business partner of DH RegSys - Conducting Clinical Investigations in Vietnam and Thailand
Ivon Septriyana, Clinical Project Manager S-E Asia, MD-Clinicals - Q&A session
Access provided by WMDO.ORG
THURSDAY, JUNE 24 11:00am-1:30pm CEST
AUSTRALIA & NEW ZEALAND
- Medical Device Regulatory Requirements in Australia and New Zealand
Jean Boudaud, Brandwood CKC - Opportunities Conducting Clinical Investigations in Australia and New Zealand
Suzanne Williams, Mobius Medical - Corporate Structures and Tax Incentives: Optimising your Clinical Trials in Australia
Blair Lucas, Acclime - Q&A session
Access provided by WMDO.ORG
THURSDAY, AUGUST 26 11:00am-1:30pm CEST
KOREA & JAPAN
- Update on Medical Device Regulatory Requirements in Korea
Rachel Chung, Synex Consulting Ltd. - Conducting Clinical Investigations Pre- and Post-Market in Korea
Kim Young, Synex Consulting Ltd. - Update on Medical Device Regulatory Requirements in Japan from the viewpoint of Registered Certification Body under PMD Act
Junya Onae, BSI Japan - Conducting Clinical Investigation Pre-and Post-Market in Japan from the viewpoint of Registered Certification Body under PMD Act
Junya Onae, BSI Japan - Q&A session
Access provided by WMDO.ORG
THURSDAY, SEPTEMBER 9 11:00am-1:30pm CEST
CHINA & TAIWAN
- Latest Update on Market Access Requirements in China
Li Xin, Clinical Project Manager, MD-Clinicals - Conducting Clinical Investigations in China
Li Xin, Clinical Project Manager, MD-Clinicals - Conducting Clinical Investigations in Taiwan
Ivon Septriyana, Clinical Project Manager S-E Asia, MD-Clinicals - Taiwan Medical Device Regulatory Requirements Update
Jenny Lin, PharmaLex - Market Entry Considerations for Mainland China
Maxime Van 't Klooster, Acclime - Q&A session
Access provided by WMDO.ORG
THURSDAY, SEPTEMBER 16 11:00am-1:30pm CEST
MIDDLE EAST
- Regulatory System for Medical Devices in Saudi Arabia
Yazeed Mohammed Alduhayan, Regulatory expert - Regulatory System for Medical Devices in Middle East Arab Countries - Update
Yazeed Mohammed Alduhayan, Regulatory expert - Industry Persepective of Bringing a Medical Device to the Middle East Market
Yazeed Mohammed Alduhayan, Regulatory expert - Conducting Clinical Investigations in Middle East Arab Countries
Yazeed Mohammed Alduhayan, Regulatory expert - Q&A session
Access provided by WMDO.ORG
THURSDAY, novEMBER 11 3:00Pm-5:30pm CEST
SOUTH AMERICA
- Overview of Medical Device Regulations in Brazil and Argentina
Marcelo Autunes, SQR Consulting - Including Brazil and Argentina in Global Clinical Investigations
Juliana Castro, RARAS CRO - Overview of Medical Device Regulations in Mexico and Chile
Marcelo Autunes, SQR Consulting - Conducting FIM studies in South America
Juliana Castro, RARAS CRO - Q&A session
What makes the Global Medical Device Focus 2021 the hottest event of the year?
The world's top medical device experts
The Global Medical Device Focus 2021 brings you face-to-face with local experts from around the world to discover what it takes to successfully plan, implement and obtain medical device registration throughout Asia Pacific, Middle East, and South American markets.
The latest expert knowledge and insight
Come join the medical device industry's leading experts and authorities in clinical research and regulatory affairs for an exciting program of discovery and exchange. With a diverse array of topics and discussions to choose from, there's something for everyone at the Global Medical Device Focus 2021.
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