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2020 Workshop: Regulation of In Vitro Diagnostic Devices (Conducted Remotely)

In Vitro Diagnostic (IVD) devices are a key component of healthcare, and pivotal to advancing technology solutions for patient centric care, such as personalized medicine. The workshop will provide a fundamental understanding of the principles behind effective regulation of IVD devices, and cover an overview of the technical documentation and available international standards. This enables an informed decision when planning for the development, market entry and management of IVD devices.


              

         




Date and Time


01 Sep 2020 @ 08:30 - 02 Sep 2020 @ 17:30

Registration


Registration is closed

Speaker


John Thornback

Dr John Thornback

Chief Operating Officer
Diagnostics Development Hub

Adelheid_Schneider


Dr Adelheid Schneider

Head
Quality and Regulatory Asia Pacific
Roche Diagnostics Asia Pacific Pte Ltd 

Varun Veigas

Mr Varun Veigas

Regional Manager
Regulatory Affairs Asia Pacific
Roche Diagnostics Asia Pacific Pte. Ltd

Sumati Randeo

Ms Sumati Randeo

Head External Affairs
Roche Diagnostics India

Joyce tan

Ms Joyce Tan

Director
Regulatory Affairs SEA
BD

Maple Ye Hongye

Dr Maple Ye Hongye

Senior Manager
Diagnostics Development Hub

Kelsen Bastari

Dr Kelsen Bastari

Senior Regulatory Specialist
Medical Devices Branch
Health Sciences Authority

Photograph_Beverly Liew

Ms Beverly Liew

Senior Regulatory Specialist
Medical Devices Branch
Health Sciences Authority

Danny Ong

Mr Danny Ong

Senior Regulatory Specialist
Medical Devices Branch
Health Sciences Authority

shelley tang

Ms Shelley Tang

Principal
Stellar consulting