Innovit

Solving global problems in UDI, GDSN, PIM & MDM for Medical Device suppliers and Healthcare Providers with 'validated' data management/syndication systems.

[Innovit @InnovitMDM]

About ten regulatory agencies will publish new UDI requirements in the next five years. Is your global UDI strategy in place and ready to scale? Join our webinar to learn the 'Top 12 Things to Prepare for Your Global UDI Journey'. Register today: https://t.co/Xw34rlfazZ

[Innovit @InnovitMDM]

Not sure where to start on your journey to global UDI compliance? Join us for our upcoming webinar with guest speaker Wes Bloemker, formerly of Arthrex and learn the 'Top 12 Things to Prepare for Your Global UDI Journey'. Register today: https://t.co/PwCfsJbbFZ

[Innovit @InnovitMDM]

The U.S., Europe, China, South Korea, Saudi Arabia...the list goes on and on. At least ten regulatory agencies will publish new UDI requirements in the next five years! Find out how to map out your UDI strategy from a global perspective in our most recent blog.

[Innovit @InnovitMDM]

Success! Our client, a global medical device company and leader in orthopedic devices, was the first to successfully complete M2M testing with the TGA’s AusUDID! Learn how their efforts allowed them to meet the stringent regulatory requirements in our most recent blog post.

[Innovit @InnovitMDM]

2023 is in full swing and we've got a lot to be excited about. Innovit has big plans for the year! Get caught up with us and learn what's coming!

[Innovit @InnovitMDM]

We couldn’t be more excited about 2023, but before we look to the promising year ahead (in part two of this blog series), we wanted to wrap up the prior year by sharing a recap of all of our accomplishments.

[Innovit @InnovitMDM]

Don't miss out on the opportunity to benefit from our GUDID experience! Join us Thursday, November 17th to walk through the steps to set up an M2M connection - and hear the lessons we've learned along the way. Register Now: https://t.co/YuZ0E8XpQd

[Innovit @InnovitMDM]

Have a significant number of records to submit to GUDID? Planning to manage those via manual entry? You might consider establishing an M2M connection for your organization. Join our webinar to walk through the steps to set-up a connection. Register Now: https://t.co/cULdTZFyAD

[Innovit @InnovitMDM]

Participants in our "9-Steps to GUDID Class I Medical Device Compliance" webinar had a lot of great questions about how to navigate the path to compliance. We captured those questions and answers in this blog for others who may need similar guidance. https://t.co/Yqt4hpysiS

[Innovit @InnovitMDM]

After 3 delays, the date for Class I devices to comply with the FDA's GUDID requirements is just months away on Dec 8, 2022. Join our webinar '9-Steps to GUDID Class I Medical Device Compliance' for a walkthrough of the path to compliance. Register now: https://t.co/5Ga5ltWHbX

[Innovit @InnovitMDM]

Brazil’s medical device market regulator, ANVISA has announced major updates to its Resolution of the Collegiate Board of Directors (RDC) 185/2001. Read the full article for a summary of the changes, which take effect March 1, 2023. https://t.co/ZoajOAtqyO

[Innovit @InnovitMDM]

Newsflash! FDA Issues Final Guidance on UDI Compliance Requirements and Extends Enforcement Deadline. Read our blog to learn more!
https://t.co/1a9YCOgelU

[Innovit @InnovitMDM]

Introducing an out-of-the-box solution to improve master data consistency, streamline data governance processes and publish validated data effortlessly with trading partners via the GDSN. Learn more: https://t.co/QSrUxhVd55

[Innovit @InnovitMDM]

With less than 180 days until the FDA's Class I GUDID data submission deadline, you're going to want to bookmark this page for all the documentation, training and tools you need to successfully navigate your journey to compliance! https://t.co/OPXiCp9Ifv

[Innovit @InnovitMDM]

Anyone else looking forward to connecting again in person? Here is the line-up of Innovit events for 2022. We hope to see at one or more!
https://t.co/tA2SRZRaGy

[Innovit @InnovitMDM]

Our team is looking forward to connecting in-person with our colleagues and peers at the June 2022 GS1 Connect Conference. Care to join us? Use our code: 22EXH10-AA-108 to get 10% off the cost of registration. Hope to see you in sunny San Diego!
https://t.co/qfFHKj339N

[Innovit @InnovitMDM]

Only 227 days remain until the FDA's Class I GUDID deadline arrives! Need to know more? Get all your questions answered in our new blog.
https://t.co/njZ10V1Vgt

[Innovit @InnovitMDM]

Announcing Innovit's new EUDAMED Reference Center! All the documentation and training videos you need to successfully prepare for and comply with EUDAMED, in one convenient location. Check it out today...bookmark it for tomorrow! https://t.co/iHjJ3vhtJx

[Innovit @InnovitMDM]

That's a wrap for 2021! It was a busy year at Innovit, with an even busier 2022 in the works! Check out some of our most memorable accomplishments from the year past and read about the exciting initiatives we have planned for the year ahead. https://t.co/qvTEpiaEoB

[Innovit @InnovitMDM]

Join a group of EUDAMED subject matter experts and secure your path to compliance!
https://t.co/UwqKzs1w9g