atrify becomes 1WorldSync
At atrify, we always strive to offer our customers the best possible solutions. Following the acquisition by 1WorldSync, we have been thinking hard about our future strategy and would now like to share some significant news with you. Our goal has been to...
EUDAMED is the central information system developed by the European Commission to increase transparency and improve traceability of medical devices in the European Union. As the UDI module is already in production environment...
The introduction of EUDAMED has a significant impact on supply chain management in the medical device industry. However, these positive effects can only be optimized if they are combined with a strategy for exchanging product information with...
I am honored to have been invited as a speaker for the MedTech Europe webinar on EUDAMED, which took place at the end of March. The webinar was organized specifically for the MedTech industry and had over 1,000 registered participants, a...
We tell you how you can close this gap! In many gap analyses we have conducted, we have found that medical device manufacturers are missing on average about 60% of the data required by EUDAMED. This shows how important it is to...
The EU Medical Device Regulation (EU MDR) covers certain beauty products that were previously not considered medical devices. This means that these products must now meet the same safety and efficacy standards as conventional medical devices.The...
On Dec. 9, the European Commission announced the extension of the validity period of certificates for legacy products on the European market. This has caused uncertainty and perplexity among some medical device manufacturers regarding the...
The AdvaMed MedTech Conference is the top event for medtech professionals. World-class speakers, an informative program, networking with professionals from the medtech industry and plenty of business opportunities make the Medtech Conference an event that medtech...
Visit atrify at our joint booth TT-14 with USDM Life Sciences at RAPS Convergence, September 11-13, 2022 in Phoenix, Arizona. RAPS Convergence is the world's largest annual gathering of professionals and innovators in the field of...
Visit atrify at booth 529 at the AHRMM22 Conference & Exhibition, August 7-10, 2022 at the Anaheim Convention Center in Anaheim, California.The AHRMM22 Conference & Exhibition is the premier showcase for the latest products, solutions,...
I'm very happy to confirm that for the second year, our representative Lionel Tussau has been reelected Member of the GS1 Healthcare Leadership Team, in charge of leading the strategy of GS1 worldwide for this industry. We thank the community for their vote of...
We'd like to remind you that all medical devices sold in Finland must be registered in EUDAMED (UDI module) - whether new or "legacy devices" - since 2021; and the same will apply to IVD legacy devices by August 2022 already! With atrify, you can easily comply with...
Even if the mandatory registration of medical devices in EUDAMED still seems a long way off until 2023, many experts recommend already dealing with the complex requirements now and start testing and registering in time. GS1 Norway officially recommends using the...
Lionel Tussau, the head of atrify Healthcare Market Unit, will participate in the round table organized by the Italian Trade Association Confindustria Dispositivi Medici during the Regulatory Affairs Days on 27th May (digital event), to share the expertise of the...
We are pleased to finally be back at the MedTech Forum and to welcome you to the largest healthcare and medical technology conference. Be there when experts talk about the latest trends and developments in healthcare and technology....
For the last few months, you have been the "happy" project leader for Eudamed! The one who inherited this project that nobody wanted... This topic has already put you in a cold sweat, just trying to get your famous SRN... Now that the UDI module is live (since last...
After years of zoom meetings, it was great to see so many of you in real life. This year's conference was heavily focused on the Scan 4 Safety project, for which atrify provides the GDSN data pool. Healthcare in the UK is starting to move forward beyond COVID, but...
In this release, the focus is on: Verified Recipients, CIN Process optimisation Change Application Type of change Added value for you Introduction of a new publication target publishing and datapool Improvement in the maintenance of publication targets More transparency about...
We are pleased to announce that the partnership between GS1 Austria and atrify will be strengthened again. Especially manufacturers of medical devices located in Austria can benefit from the close cooperation between GS1 Austria and atrify. From now on, they have the...
Finally, the live events are back! atrify will have a stand at the GS1 UK Healthcare Conference in London on 17 and 18 March 2022. This year, the focus will be on how GS1 standards are being used to improve patient safety and...
After its consultation on the UDI regulation in the UK, the MHRA is now holding another consultation on the Clinical trial regulation to improve processes and simplify the activity of clinical trial sponsors. Its focus is particularly on "clinical trials and the...
Hosting a forum during a pandemic can be quite a challenge, especially when the participants are from the health sector. TÜV Süd, a notified body, has risen to the challenge and made the best of the...
The EUDAMED UDI module for the registration of medical devices has been in operation since 4 October 2021 - voluntary from the point of view of the European regulation, mandatory or almost mandatory according to various European member states. Reminder: 5 years...
Some time ago, we called on our colleagues internally to contact us with non-profit associations that need support. Many associations have experienced a very long lean period since the beginning of the pandemic, without regular operations and with less...
The UK regulator MHRA has launched an official Consultation on their future UDI regulation due to close on 26th November 2021. The regulation is expected to enter into force in July 2023. The consultation itself is very thorough, looking at a number of options for...
The Chinese authorities have confirmed that all remaining Class III medical devices must be registered in the CUDID (NMPA UDI database) by 1 June 2022 - 8 months from now. atrify has been associated with the CUDID for years. The...
Following the release of the Actor module, which has been operational since December 2020, the UDI and CERTIFICATE modules went live in EUDAMED on Monday 4 October. This is another important step towards the implementation of EUDAMED and the MDR/IVDR....
As an ongoing effort to provide information on regulations, atrify hosts online sessions in multiple languages on EUDAMED, UDI regulations, and the exchange of product content between trading partners. @GP and atrify are hosting a joint online session "UDI, EUDAMED,...
For the 6th time, atrify is saying: Welcome to the new apprenticeship year! atrify has been successfully training apprentices for several years - and now even in four different apprenticeship professions. For "IT specialist for application development", ...
Language as the basis of communication For an internationally operating company like atrify, with employees and customers all over the world, language exchange is not only the basis for success. The corporate culture that is so important to us is also...
Just recently, Timo successfully completed his training as an IT specialist for system integration with us by passing his final exam at the IHK. Timo started his training at atrify just under three years ago and we are very pleased...
My school internship was supposed to have taken place last year, but was postponed to this year due to the Corona pandemic, so I started my three-week internship in the marketing department at atrify in June 2021. Since my father works at...
Cologne, 01 July 2021. Today, the Competence Centre Data Quality of GS1 Germany was launched. The aim is to work together with industry and trade to address the issues surrounding data quality even more strongly and holistically. With the data quality service GS1 DQX...
Healthcare manufacturers will have 1 more chance to participate in the EUDAMED playground for UDI & Device registration module which will be opened by the European Commission at the end of July and run during the month of August, enabling direct interaction with...
As an ongoing effort to provide information on regulations, atrify hosts online sessions in multiple languages on EUDAMED, UDI regulations, and the exchange of product content between trading partners. @GP and atrify are hosting a joint online session "UDI, EUDAMED,...