Technology Track D: Plastic Innovation Theatre

Technology Track D: The 3rd Session of Pack&Ster Hub

MDiT Forum and Regulation Summit 2019——

Technology Track D: The 3rd Session of Pack&Ster Hub

Afternoon of Sep 25, 2019 | Conference Room X, B2 of SWEECC

Organizer: Medtec China

Conference Background

Along with the 2016-ISO 13485 release and update of new medical device GMP, the requirement on sterilization medical device packaging is stricter. What’s more, medical device manufacturers pay more attention on packaging and sterilization.

How to ensure the product quality and maintain product life, how to reduce cost and improve sterile level in packaging process and how to complete sterilization process utilizing the latest testing and sterilization method are the common issue for manufacturers and packaging suppliers.
Packaging exhibitors in Medtec China and global not only provide the advanced techniques and service, also devote to improve quality of sterile product. Due to success of the 2017 and 2018 conferences, this year’s conference will continue to combine the requirement from manufacturers and suppliers, together with the Medtec global resources to explore the testing, technology and approaches of medical device packaging and sterilization.

Conference Content

Regulatory standard system and compliance of sterilization medical device packaging in China
Packaging and quality: the requirements for packaging from manufacturers
Testing techniques in packaging and validation processes
Radiation sterilization: discussion of new options, test packaging and errors
Update of ethylene oxide sterilization technology

Who Should Attend?

Quality, Process Validation, Supplier Management, Sterilization Packaging, Production and Technology Department, Project Manager/Director and Managing Director from medical devices manufacturers