LORENZ Press Releases

Press Releases

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FDA affirms award of eCTD Contract to LORENZ



Philadelphia, 03 October 2017 // LORENZ Life Sciences Group is pleased to announce that the U.S. Food and Drug Administration (FDA) has affirmed its prior award to LORENZ of a contract for “Electronic Common Technical Document (eCTD) Validation and Review Software.” To learn more about the original contract award, please see our prior announcement here.

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LORENZ userBridge.17 conference is already completely sold out!



Frankfurt/Main, 26 July 2017 // LORENZ is pleased to announce that the userBridge.17 conference is completely sold out, eight weeks before the start of the event!

The 15th annual userBridge conference offers a unique opportunity for Regulatory Affairs professionals to catch up on latest developments in the sector, to exchange experiences with colleagues from around the globe in a relaxed setting, and to better understand LORENZ products.

“It is the secon...

userBridge.17 in Nice, France from 19-21 September 2017: Save the date and register now!



Frankfurt/Main 7 June 2017 // The Boscolo Plaza in Nice, France will be the setting for userBridge.17, the annual regulatory affairs conference hosted by LORENZ Life Sciences Group. Running from 19-21 September 2017, this forum is well-known for showcasing the very latest thinking from the world of regulatory affairs, with high-level speakers recruited to give a wide range of e...

LORENZ and Generis announce the integration of their LORENZ docuBridge and CARA products to support regulatory publishing from Documentum



Sarasota, FL / Frankfurt/Main, 28 March 2017 // Generis Knowledge Management Inc. and LORENZ Life Sciences Group today announced that they started a new joint solution integrating their two products CARA and LORENZ docuBridge to support regulatory publishing from Documentum.

This strategic partnership means that Generis and LORENZ can give customers the ability to author and publish with two industry-leading solutions: CARA for authors, and docuBridge for publishers. ...

State Institute for Drug Control (SÚKL) of Czech Republic will review electronic submissions using LORENZ docuBridge



Praha, 10 November 2016 // The LORENZ docuBridge software solution has been selected by the SÚKL (State Institute for Drug Control) located in Praha, Czech Republic for that agency’s work in receiving, reviewing and processing electronic applications for market authorizations. The SÚKL will combine docuBridge with the LORENZ Automator service for the automated download of electronic submissions from the EMA CR.

“We’re very proud that th...

Interoperable systems and standards are the hot topics at userBridge.16 conference



Frankfurt/Main, 19 October 2016 // Hamburg, a seafaring city with a long tradition of international trade was the setting for this year’s userBridge conference, the global e-regulatory affairs gathering organized by the LORENZ Life Sciences Group, the world’s premier supplier of eCTD solutions. Held from 20-22 September, the sold-out userBridge.16 event attracted 172 participants from 21 countries. Interoperability of systems and the importance of converging...

FDA awards LORENZ eCTD Contract



Philadelphia, 07 October 2016 // LORENZ Life Sciences Group is pleased to announce that the U.S. Food and Drug Administration (FDA) awarded LORENZ with an “Electronic Common Technical Document (eCTD) Validation and Review Software” contract on September 30, 2016 through a competitive procurement process.

LORENZ will implement its docuBridge, eValidator and Automator solutions in FDA’s Center for Drug Evaluation and Research (CDER) and Cent...

Two South African companies qualify for the LORENZ docuBridge 1K Club



Pretoria and Frankfurt/Main, 30 September 2016 // LORENZ Life Sciences Group is happy to introduce the latest members to the 1K Club and the first to qualify in Africa. DI Regulatory Consultants and MRA Regulatory Consultants have both recently announced they have compiled over 1,000 submissions using the LORENZ docuBridge system.

"Africa is very quickly adopting the CTD as the standard structure,” said Robyn Daniel, Director at MRA Regulatory Consultants...