Register Now: Regulatory and Commercial Product Management Webinars
Dear Valued Member,
As the leading trade association for the optical industry, The Vision Council aims to arm its members with the key information and resources needed to run a successful business. With this in mind, The Vision Council has partnered with Reed Technology and Information Services Inc. (Reed Tech) to provide members with a connection to a full-service solution to manage regulatory and commercial product information, including help with Unique Device Identifier (UDI) submissions.
This is an important topic for our members as the FDA Class I UDI requirements for labeling, direct marking and AccessGUDID submission are due next September. Additionally, for those manufacturers intending to market prescription eyewear products in the European Union, the European Union Databank on Medical Devices (EUDAMED) submission will be due in May 2022. Furthermore, additional global regulators are emerging and will require regulatory expertise for UDI submissions.
We encourage members to take advantage of this benefit by attending the upcoming webinars conducted by Reed Tech on this important topic. The second webinar will take place on April 28, 2020 and will provide attendees with the tools and know-how to make the submission process as smooth as possible, and allow for questions and discussions surrounding the topic. The webinar will cover the following topics:
- Class I Template
- EU MDR Basic requirements for UDI
- How Reed Tech can help you
For more information on the upcoming webinars and to register, please click here.
For more information on The Vision Council's partnership with Reed Tech, please visit thevisioncouncil.org.